CDWAH-U / Stainless steel re-usable holder of great resistance and durability. The holder is designed to be fixed on the tray, which allows reproducible location of the cleaning indicator in ultrasonic washing machines. Base: 32,7 mm wide, 72,5 mm long. Designed to hold Chemdye® CDWA cleaning indicators and perform routine control of cleaning processes in ultrasonic washers. Characteristics: Chrome plating SUS304 grade stainless steel re-usable holder of great resistance and durability. Base: 32 mm wide, 72.5 mm long, pin at the back side. The holder is designed to be fixed on the tray, which allows reproducible location of the cleaning indicator in ultrasonic washing machines, without representing a challenge to the washing process. Specifications: Process: Cleaning and thermodisinfection Regulations: ISO/TS 15883-5

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Holder for cleaning and thermodisinfection Indicators. Stainless Steel re-usable holder of great resistance and durability. Base: 32 mm wide, 72 mm long, pin at the back side. ISO/TS 15883-5. Designed to hold Chemdye® CDWA and Integron® IT27W indicators in order to perform routine control of cleaning and thermal disinfection processes in automatic machines. Characteristics: Chrome plating SUS304 grade stainless steel re-usable holder of great resistance and durability. Base: 32 mm wide, 72.5 mm long, pin at the back side. Basket: 32 mm wide, 37 mm long, 0.5 mm thick. The holder is designed to mimic the cleaning challenges posed by a large process load during the washing cycle and can be fixed on the tray, which allows reproducible location of the cleaning indicator in the washer-disinfector. When CDWA4 is placed within the holder, half of the test soil is obscured, thus simulating the joint of a surgical instrument, with water stream hitting it indirectly. The other half of the test soil is covered by a mesh, thus posing a difficulty for water stream to reach it, mimicking shadowed or occluded surfaces. The new design of CDWAH optimizes the control of the washer disinfectors ability to force water and detergent into and onto the test soil. Specifications: Process: Cleaning and thermodisinfection Regulations: ISO 15883

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Instructions For Use: Before The Test: Place the holder around the neck of the capsule. Press the holder down so that the groove of the holder fits securely around the neck of the vial. Insert the L shaped end on either side of the holder into the holes of the Ultrasonic device’s basket to hold the vial in position. The holder can be attached to a wire basket or perforated basket. Vials should be placed in the correct location within a tray / basket according to Ultrasonic Cleaning Indicator´s IFU based on the size of the tank. After the test is complete After the ultrasonic cycle remove the vial holding it with three fingers of one hand and the index finger and thumb of the other hand on the holder and lid of capsule. Place the index finger on the end of the holder, then place the thumb on the lid of the capsule for support, push the holder back off the neck of the capsule and remove the holder with both fingers.

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CDWA4 / Cleaning Indicator for cleaning performance tests. Challenge level: very high. Detects all the factors that affect the result of a washing process. Initial Color: Fuchsia. Result: removal of the fuchsia organic substance. Designed for routine control of cleaning processes and for monitoring automatic washing machines effectiveness as well as monitoring ultrasonic washing machines which operate at frequencies equal to or greater than 35 kHz, and temperatures between 30 ºC and 70 ºC. Characteristics: Challenge Level: Very high. Allows detection of all factors affecting the outcome of cleaning process. Initial Color: Fuchsia. Size: 70 mm x 30 mm (approximate). Synthetic temperature-stable support. Result: Elimination of fuchsia organic substance. To interpret results visually, use the results reference guide on product´s instructions for use. Optionally, the readout of the cleaning indicator can be done using Trazanto Automatic Quality Control and Traceability System (see instructions for use in device´s manual). Instructions For Use: Choose the Chemdye® Splat CDWA indicator according to the desired difficulty. Place the indicator on the Chemdye® Splat CDWAH or Chemdye® Splat CDWAH-U holder. Place the system on the tray along with the material. Once the cleaning cycle is over, remove the indicator. Analyze Chemdye® Splat CDWA indicators using the reference table and record results. If unfavorable results are obtained, perform the appropriate corrective actions and repeat the washing process. Specifications: Process: Cleaning and thermodisinfection Initial Color: Fuchsia Regulations: ISO 13485, ISO/TS 15883-5

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Super Rapid Self-contained Biological Indicator for Steam sterilization processes. Geobacillus stearothermophilus (ATCC 7953) 10^6 spores per vial. Readout: 1 hour. An optional visual pH color change confirmation could be made after 48 hours of incubation. If sterilization process has not been successful, culture medium will change to a greenish color first, and then to yellow during incubation at 60 ºC, thus showing the presence of living spores. If sterilization process is successful culture medium will remain purple after the incubation process. 7-day readout is optional and not intended to be routinely performed; it is an initial validation of the 1 hour-reading. Fluorescence results may be compared to the 7-day visual reading. Note: if 7-day readout is performed, a humidified environment will be required to avoid medium to dry out. D-Value: Not lower than 1.5 minutes at 121 ºC. Another D-value is informed at 132 ºC and at 135 ºC. Z-Value is informed. Instructions For Use: Identify the Terragene® Bionova® BT222 SCBI by writing the sterilizer number (in case of having more than one), load number and processing date on the label. Pack the SCBI along with materials to be sterilized in an appropriate package according to recommended sterilization practices. Place the package in those areas which are considered most inaccessible for the sterilizing agent (e.g., the center of the load and areas near the door). Sterilize as usual. After the sterilization process has finished, open the sterilizer door, wait five minutes and remove the SCBI from the package. CAUTION: Wear safety glasses and gloves when removing the Terragene® Bionova® BT222 SCBI from the sterilized package. WARNING: Do not crush or handle the SCBI excessively, since this might cause the glass ampoule to burst. Let the SCBI cool down until it reaches room temperature. Check the Process Indicator on SCBI label. A color change to brown indicates that the SCBI has been exposed to Steam. IMPORTANT: This color change does not evidence the process effectiveness to achieve sterility. If the Process Indicator color has not changed, check the sterilization process. Press the lid to seal the tube. Crush the ampoule contained in the SCBI with an individual ampoule crusher or with the ampoule crusher placed within the incubator´s incubation area. Then shake the tube down vigorously, with movements similar to those performed to lower the temperature in a mercury thermometer, until the medium reaches the base of the tube and soaks the spore carrier entirely. Finally, place the SCBI in the incubator. Incubate the processed indicator and the positive control indicator in the appropriate Terragene® Bionova® Auto-Reader Incubators for a maximum of 1 hour at (60 ± 2) °C for super rapid readout. Specifications: Process: Steam Microorganism: Geobacillus stearothermophilus (ATCC 7953) Population: 10^6 Spores/carrier Read-Out Time: 1 h Regulations: IRAM 37102-1, IRAM 37102-3, ISO 11138-1, ISO 11138-3

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Rapid Self-contained Biological Indicator for Ethylene Oxide sterilization processes. Bacillus atrophaeus (ATCC 9372) 10^6 spores per vial. Readout: 4 hours. An optional visual pH color change confirmation could be made after 48 hours of incubation. If sterilization process has not been successful, culture medium will change to a greenish color first, and then to yellow during incubation at 37 ºC, thus showing the presence of living spores. If sterilization process is successful culture medium will remain blue after the incubation process. 7-day readout for visual confirmation by color change is optional and not intended to be routinely performed; it is an initial validation of the 4 hour-reading. Fluorescence results may be compared to the 7-day visual reading. Instructions For Use: Identify the Terragene® Bionova® BT110 SCBI by writing the sterilizer number (in case of having more than one), load number and processing date on the label. Pack the SCBI along with materials to be sterilized in an appropriate package according to recommended sterilization practices. Place the package in those areas which are considered most inaccessible for the sterilizing agent (e.g., the center of the load and areas near the door). Sterilize as usual. After the sterilization process has finished, open the sterilizer door, wait five minutes and remove the SCBI from the package. CAUTION: Wear safety glasses and gloves when removing the Terragene® Bionova® BT110 SCBI from the sterilized package. Check the Process Indicator on SCBI label. A color change to green indicates that the SCBI has been exposed to Ethylene Oxide. IMPORTANT: This color change does not evidence the process effectiveness to achieve sterility. If the color of the Process Indicator has not changed, check the sterilization process. Press the lid to seal the tube. Crush the ampoule contained in the SCBI with an individual ampoule crusher or with the ampoule crusher placed within the incubator´s incubation area. Then shake the tube down vigorously, with movements similar to those performed to lower the temperature in a mercury thermometer, until the medium reaches the base of the tube and soaks the spore carrier entirely. Finally, place the SCBI in the incubator. Incubate the processed indicator and the positive control indicator in the appropriate Terragene® Bionova® Auto-Reader incubators for a maximum of 4 hours at (37 ± 2) °C for rapid readout. Note: Holding time between sterilization and incubation should not exceed a 7-day period. Fluorescence detection by the reader (excitation 340-380 nm / emission 455-465 nm) means failure in the sterilization process. If no fluorescence is detected after 4 hours of incubation, the result is negative. The positive control must give positive fluorescence readout. It is good practice to incubate a positive control for visual color change. If chamber relative humidity is unknown or < 35 %, continue to incubate the Biological Indicator for a pH color change result, since low relative humidity may increase the fluorescent readout time beyond 4 hours. Specifications: Process: Ethylene Oxide Microorganism: Bacillus atrophaeus (ATCC 9372) Population: 10^6 Spores/carrier Read-Out Time: 4 h Regulations: IRAM 37102-1, IRAM 37102-2, ISO 11138-1, ISO 11138-2 Length: 40 mm

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Hyper Rapid Self-contained Biological Indicator for Vaporized Hydrogen Peroxide sterilization processes. Final readout: 5 minutes. Indications For Use: Terragene® Bionova® BT98 fluorescence hyper rapid readout Biological Indicators have been designed for quick and easy monitoring of Plasma or vaporized hydrogen Peroxide sterilization cycles. Device Description: Terragene® Bionova® BT98 fluorescence hyper rapid readout Biological Indicators are single-use Self-Contained Biological Indicators (SCBIs) that consist of a polypropylene tube, a spore carrier and a glass ampoule with a culture medium, enclosed with a colored cap. Each tube contains a population of Geobacillus stearotermophilus ATCC 7953 spores inoculated on a spore carrier, a plastic cap with holes and a barrier permeable to Plasma or Vaporized Hydrogen Peroxide. Each BT98 has a Process Indicator on label that changes from purple to green when exposed to hydrogen peroxide. Precautions: Warning: Do not use Terragene® Bionova® BT98 SCBI to control EO, Dry Heat, Formaldehyde or other sterilization processes different from specified. Do not reuse SCBI. Warning:  Place one or more SCBI in sterilizing hard-to-reach areas to ensure all areas of the chamber are sterilized. Please evaluate all load configurations to ensure ALL hard-to-reach areas have been identified, and place a SCBI in each of those locations. Warning:  Do not reuse the sterilizer until the SCBI test result is negative. Instructions For Use: Identify the Terragene® Bionova® BT98 SCBI by writing the sterilizer number (incase of having more than one), load number and processing date on the label. Pack the SCBI along with materials to be sterilized in an appropriate package according to recommended sterilization practices. Place the package in those areas which are considered most inaccessible for the sterilizing agent (e.g., the center of the load and areas near the door). Sterilize as usual. After the sterilization process has finished, open the sterilizer door, wait five minutes and remove the SCBI from the package. Caution Wear safety glasses and gloves when removing the Terragene® Bionova® BT98 SCBI from the sterilized package. ( Do not crush or handle the SCBI excessively, since this might cause the glass ampoule to burst. Let the SCBI cool down until it reaches room temperature.) Check the Process Indicator on SCBI label. A color change to green indicates that the SCBI has been exposed to Hydrogen Peroxide. IMPORTANT: This color change does not evidence the process effectiveness to achieve sterility. If the color of the Process Indicator has not changed, check the sterilization process. Press the lid to seal the tube. Crush the ampoule contained in the SCBI with an individual ampoule crusher or with the ampoule crusher placed within the incubator´s incubation area. Then shake the tube down vigorously, with movements similar to those performed to lower the temperature in a mercury thermometer, until the medium reaches the base of the tube and soaks the spore carrier entirely. Finally, place the SCBI in the incubator. Incubate the processed indicator and the positive control indicator in the appropriate Terragene® Bionova® auto-reader incubators for a maximum of 5 minutes at (60 ± 2) °C for hyper rapid readout. (Holding time between sterilization and incubation should not exceed a 1-hour period.) Important: Use a non-sterilized SCBI as a positive control at least once per day, when a sterilization cycle is run. The positive control ensures that correct incubation conditions were met; the capability of the medium to promote rapid growth; viability of spores has not been altered due to improper storage temperature, humidity or proximity to chemicals and proper functioning of Terragene® Bionova® Auto-Reader Incubators. Both, the positive control indicator and the processed indicator, should belong to the same batch. Fluorescence detection by the reader (excitation 340-380 nm / emission 455-465 nm) means failure in the sterilization process. If no fluorescence is detected after 5 minutes of incubation, the result is negative. The positive control must give positive fluorescence readout. It is good practice to incubate a positive control for visual color change. Record positive results and discard the SCBIs immediately, as it is indicated below. Hyper Rapid Readout: 5 minutes The hyper rapid readout must be carried out in the appropriate Terragene® Bionova® auto-reader incubators. Fluorescence is emitted after the reader stimulates the spore carrier with UV light. Final readout of negative results is readily available after 5 minutes of incubation. Fluorescence readout is an indirect measure of the viability of Geobacillus stearothermophilus spores after the sterilization process (positive results). Furthermore, a failure in the sterilization process can also become evident by culture medium color-change. Due to the high sensitivity of the fluorescence results at 5 minutes, conventional incubation for color change of Terragene® Bionova® SCBI BT98 is not an advantage. Visual Confirmation: 5 days: Optionally, you can perform a visual color-change confirmation after a 5-day incubation. If the sterilization process has not been successful, culture medium will turn to yellow during incubation at (60 ± 2) ºC, indicating the presence of living spores. If sterilization was successful, culture medium will remain purple after incubation. The positive control must show a color change from purple to yellow for results to be valid. ( If 5-day readout is performed, a humidified environment will be required to prevent medium from drying out.) Readout Time: 7 days A 7-day readout is optional and may be routinely performed. This is an initial validation of the 5-minute readout. Fluorescence results are compared to the 7-day visual readouts. Monitoring Frequency: Follow facility policies and procedures which should specify a biological indicator monitoring frequency compliant with professional association recommended practices and/or national guidelines and standards. As the best practice and to provide optimal patient safety, Terragene® recommends that every sterilization load be monitored with an appropriate biological indicator. Storage: Store in a dark place at temperature between 10-30 ºC and 30-80 % relative humidity. Do not freeze. Do not store biological indicators near sterilizing agents or other chemical products. Shelf Life: Biological Indicators have an expiration date of 2 years from the date of manufacture when stored at recommended conditions. Do not use indicators after their expiration date. Chemical Process Indicator on SCBI label have an expiration date of 2 years when used as part of SCBI. Endpoint Stability Reaction: Chemical Process Indicator endpoint shall remain unchanged for a period of 6 months when stored at previously indicated conditions. Disposal: Discard biological indicators after use according to your country’s healthcare and safety regulations. The positive biological indicators can be autoclaved in a gravity air displacement steam sterilizer at 121 ºC for 5 minutes, 132 ºC for 15 minutes or 134 ºC for 10 minutes; or in a dynamic air removal steam sterilizer at 132 °C for 4 minutes or 135 °C for 3 minutes. Specifications: Population: 10^6 Spores/carrier Read-Out Time: 5 min Regulations: IRAM 37102-1:1999, ISO 11138-1:2017, ISO 13485:2016 / NS-EN ISO 13485:2016

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Ultra Rapid Self-contained Biological Indicator for Steam sterilization processes. Geobacillus stearothermophilus (ATCC 7953) 10^6 spores per vial. Readout: 20 minutes. An optional visual pH color change confirmation could be made after 48 hours of incubation. If the sterilization process has not been successful, the culture medium will change to a greenish color first, and then to yellow during incubation at 60 ºC, thus showing the presence of living spores. If the sterilization process is successful culture medium will remain purple after the incubation process. 7-day readout is optional and not intended to be routinely performed; it is an initial validation of the 20 minute-reading. Fluorescence results may be compared to the 7-day visual reading. Note: If 7-day readout is performed, a humidified environment will be required to avoid medium to dry out. D-Value: Not lower than 1.5 minutes at 121 ºC. Another D-value is informed at 132ºC and at 135ºC. Z-Value is informed. Instructions For Use: Identify the Terragene® Bionova® BT224 SCBI by writing the sterilizer number (in case of having more than one), load number and processing date on the label. Pack the SCBI along with materials to be sterilized in an appropriate package according to recommended sterilization practices. Place the package in those areas which are considered most inaccessible for the sterilizing agent (e.g., the center of the load and areas near the door). Sterilize as usual. After the sterilization process has finished, open the sterilizer door, wait five minutes and remove the SCBI from the package. CAUTION: Wear safety glasses and gloves when removing the Terragene® Bionova® BT224 SCBI from the sterilized package. (Do not crush or handle the SCBI excessively, since this might cause the glass ampoule to burst. Let the SCBI cool down until it reaches room temperature.) 5. Check the Process Indicator on SCBI label. A color change to brown indicates that the SCBI has been exposed to Steam. ( This color change does not evidence the process effectiveness to achieve sterility. If the Process Indicator color has not changed, check the sterilization process.) 6. Press the lid to seal the tube. Crush the ampoule contained in the SCBI with an individual ampoule crusher or with the ampoule crusher placed within the incubator´s incubation area. Then shake the tube down vigorously, with movements similar to those performed to lower the temperature in a mercury thermometer, until the medium reaches the base of the tube and soaks the spore carrier entirely. Finally, place the SCBI in the incubator. 7. Incubate the processed indicator and the positive control indicator in the appropriate Terragene® Bionova® Auto-Reader Incubators for a maximum of 20 minutes at (60 ± 2) °C for ultra rapid readout. Important: Use a non-sterilized SCBI as a positive control at least once per day, when a sterilization cycle is run. The positive control ensures that correct incubation conditions were met; capability of medium to promote rapid growth; viability of spores has not been altered due to improper storage temperature, humidity or proximity to chemicals and proper functioning of Terragene® Bionova® Auto-Reader Incubators. Both, the positive control indicator and the processed indicator, should belong to the same batch. Note: Holding time between sterilization and incubation should not exceed a 7-day period. Fluorescence detection by the reader (excitation 340-380 nm / emission 455-465 nm) means a failure in the sterilization process. If no fluorescence is detected at 20-minute incubation, the result is negative. The positive control must give positive fluorescence readout. It is good practice to incubate a positive control for a visual color change.

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Super Rapid Self-contained Biological Indicator for Plasma or Vaporized Hydrogen Peroxide Sterilization Processes. Final readout: 30 minutes. An optional visual pH color change confirmation could be performed after 48 hours of incubation. If sterilization process has not been successful, culture medium will change to yellow during incubation at 60 ºC, thus showing the presence of living spores. If sterilization process is successful culture medium will remain purple after the incubation process. 7-day readout is optional and not intended to be routinely performed; it is an initial validation of the 30-minute reading. Fluorescence results may be compared to the 7-day visual reading. Note: If 7-day readout is performed, a humidified environment will be required to prevent medium from drying out. Instructions For Use: Identify the Terragene® Bionova® BT96 SCBI by writing the sterilizer number (in case of having more than one), load number and processing date on the label. Pack the SCBI along with materials to be sterilized in an appropriate package according to recommended sterilization practices. Place the package in those areas which are considered most inaccessible for the sterilizing agent (e.g., the center of the load and areas near the door). Sterilize as usual. After the sterilization process has finished, open the sterilizer door, wait five minutes and remove the SCBI from the package. CAUTION: Wear safety glasses and gloves when removing the Terragene® Bionova® BT96 SCBI from the sterilized package.( Do not crush or handle the SCBI excessively, since this might cause the glass ampoule to burst. Let the SCBI cool down until it reaches room temperature.) Check the Process Indicator on SCBI label. A color change to green indicates that the SCBI has been exposed to Hydrogen Peroxide. IMPORTANT: This color change does not evidence the process effectiveness to achieve sterility. If the color of the Process Indicator has not changed, check the sterilization process. 6. Press the lid to seal the tube. Crush the ampoule contained in the SCBI with an individual ampoule crusher or with the ampoule crusher placed within the incubator´s incubation area. Then shake the tube down vigorously, with movements similar to those performed to lower the temperature in a mercury thermometer, until the medium reaches the base of the tube and soaks the spore carrier entirely. Finally, place the SCBI in the incubator. Incubate the processed indicator and the positive control indicator in the appropriate Terragene® Bionova® Auto-Reader incubators for a maximum of 30 minutes at (60 ± 2) °C for super rapid readout. Important: Use a non-sterilized SCBI as a positive control at least once per day, when a sterilization cycle is run. The positive control ensures that correct incubation conditions were met; the capability of the medium to promote rapid growth; viability of spores has not been altered due to improper storage temperature, humidity or proximity to chemicals and proper functioning of Terragene® Bionova® Auto-Reader Incubators. Both, the positive control indicator and the processed indicator, should belong to the same batch. Note: Holding time between sterilization and incubation should not exceed a 7-day period. Fluorescence detection by the reader (excitation 340-380 nm / emission 455-465 nm) means failure in the sterilization process. If no fluorescence is detected after 30 minutes of incubation, the result is negative. The positive control must give positive fluorescence readout. It is good practice to incubate a positive control for visual color change. Specifications: Process: Hydrogen peroxide Microorganism: Geobacillus stearothermophilus (ATCC 7953) Population: 10^6 Spores/carrier Read-Out Time: 30 min Regulations: IRAM 37102-1, ISO 11138-1

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Indicator Tape for Plasma or Vaporized Hydrogen Peroxide Sterilization Processes. Cintape® CT40 Process Indicators (Type 1 according ISO 11140-1:2014 standard) are single-use chemical indicators that consist of a roll of self-adhesive plastic tape printed with indicator ink. These indicators have been designed to monitor Plasma or Vaporized Hydrogen Peroxide sterilization processes, ensuring adequate exposure to the sterilizing agent during the sterilization process and allowing to distinguish between processed and unprocessed items. The adhesive component of the tape allows the adhesion to different types of packaging and wraps, such as cloth, paper and plastic being easy to remove and leaving no residues. Innovative highly sensitive purple ink was developed to turn to green when the indicator is exposed to Plasma or Vaporized Hydrogen Peroxide. Endpoint condition: 50 ºC, 6 minutes, 2.3 mg/l H2O2. Indicators 100 % free of toxic heavy metals. Instructions For Use: Place within a sterilizer a wrapped package closed with Cintape® CT40 Process Indicator tape that will be sterilized by Plasma or Vaporized Hydrogen Peroxide. Perform the sterilization cycle. After the sterilization process has finished, remove the package from the sterilizer and analyze the indicator results. The indicator must turn to the reference color for considering that it was exposed to Plasma or Vaporized Hydrogen Peroxide. For reference color, please refer to Result Reference Guide. Specifications: Process: Hydrogen Peroxide Initial Color: Purple Final Color: Green Indicator Type: Type 1 chemical indicator Regulations: ISO 11140-1

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CT22 / Indicator Tape for Steam sterilization processes. Cintape® CT22 Process Indicators (Type 1 according ISO 11140-1:2014 standard) are single-use chemical indicators that consist of a roll of self-adhesive paper tape printed with indicator ink. These indicators have been designed to monitor Steam sterilization processes, ensuring an adequate exposure to the sterilizing agent during the sterilization process and allowing to distinguish between processed and unprocessed items. The adhesive component of the tape allows the adhesion to different types of packaging and wraps, such as cloth, paper and plastic being easy to remove and leaving no residues. Innovative highly sensitive yellow ink was developed to turn to dark brown / black when the indicator is exposed to Steam. Endpoint condition: 121 ºC, 10 minutes; 134 ºC, 2 minutes. Instructions For Use: Place within a sterilizer a wrapped package closed with Cintape® CT22 Process Indicator tape that will be sterilized by Steam. Perform the sterilization cycle. After the sterilization process has finished, remove the package from the sterilizer and analyze the indicator results. The indicator must turn to the reference color for considering that it was exposed to Steam. For reference color, please refer to Result Reference Guide. Specifications: Process: Steam Initial Color: Yellow Final Color: Black, Dark Brown Indicator Type: Type 1 chemical indicator Regulations: ISO 11140-1 More Info About This Product: Color Chart

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KPCD222-C / Test Pack PCD Kit. Process Challenge Device for Steam sterilization processes with moving-front Type 5 Indicator and Bionova® Super Rapid Self-contained Biological Indicator BT222, plus Bionova® BT222 Biological Indicators Positive Control. For routine load release, especially for loads containing implants. For routine sterilizer monitoring. For periodic validation of the sterilizer (after installation, repair, relocation). Detects inadequate air removal and steam penetration in dynamic-airremoval (pre-vacuum) and gravity displacement steam autoclaves between 121-135 ºC. Characteristics: The Kit Consists Of: PCD222-C: Porous cards system holding: A Self-contained Biological Indicator Bionova® BT222. A Type 5 chemical indicator Integron® IT26-C (moving-front integrator). A self-adhesive Record Card, PCDBI-C-RC, where data on sterilization cycle may be written. Self-contained Biological Indicator Bionova® BT222 (to be used as a positive control) Specifications: Initial Color: Blue Final Color: Dark Grey or Black Process: Steam Microorganism: Geobacillus stearothermophilus (ATCC 7953) Population: 10^6 Spores/carrier Read-Out Time: 1 h Regulations: ANSI/AAMI ST79, ISO 11138-1, ISO 11138-3 IT26-C Chemical Integrator (within the challenge device) The migration is visible through a zone marked ACCEPT or REJECT, thus indicating whether sterilization conditions were met. Integration condition is calibrated against the kill time of a 106 G. stearothermophilus ATCC 7953 spores€™ population, calculated in BIER (Biological Indicator Evaluator Resistometer). Conditions: saturated steam at 121 °C, 128 °C, 135 °C. BT222 Super Rapid Self-contained Biological Indicator (within the challenge device): ‰¥106 G. stearothermophilus ATCC 7953 spores per vial in paper carrier. Glass ampoule with growth indicator medium. Label with chemical indicator line printed with Steam reactive ink (Color change: pink to brown)

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KPCD224-C / Test Pack PCD Kit. Process Challenge Device for Steam sterilization processes with moving-front Type 5 Integrator and Bionova® Ultra Rapid Self-contained Biological Indicator BT224, plus Bionova® BT224 Biological Indicators Positive Control. Class 5 spores per strip. For routine load release, especially for loads containing implants. For routine sterilizer monitoring. For periodic validation of the sterilizer (after installation, repair, relocation). Detects inadequate air removal and steam penetration in dynamic- airremoval (pre-vacuum) and gravity displacement, steam autoclaves between 132-135 ºC. Characteristics: The kit Consists Of: PCD224-C: Porous Cards System Holding: A Self-contained Biological Indicator Bionova® BT224.A Type 5 chemical indicator Integron® IT26-C (moving-front integrator). A self-adhesive Record Card, PCDBI-C-RC, where data on sterilization cycle may be written. Self-contained Biological Indicator Bionova® BT224 (to be used as a positive control) Specifications: Initial Color: Blue. Final Color: Dark Grey or Black. Process: Steam Microorganism: Geobacillus stearothermophilus (ATCC 7953) Population: 10^6 Spores/carrier Read-Out Time: 20 min Regulations: ANSI/AAMI ST79, ISO 11138-3, ISO 11140-1 IT26-C Integrator Indicator (within the challenge device): The migration is visible through a zone marked ACCEPT or REJECT, thus indicating whether sterilization conditions were met. Integration condition is calibrated against the kill time of a 106 G. stearothermophilus ATCC 7953 spore population, calculated in BIER (Biological Indicator Evaluator Resistometer). Conditions: saturated steam at 121 ºC, 128 ºC, 135 ºC. BT224 Self-contained Ultra Rapid Biological Indicator (within the challenge device): 106 G. stearothermophilus ATCC 7953 spores per vial in paper carrier. Glass ampoule with growth indicator medium. Label with chemical indicator line printed with Steam reactive ink (Color change: pink to brown) Final results: by fluorescence after incubation for 20 minutes at 60 ºC (sensitivity 97%). An optional visual pH color change confirmation could be made after 48 hours of incubation. A 7-day readout is optional to confirm 20-minutes results by color change. Note: If sterilization process was not successful, indicator medium will turn yellow after incubation, thus indicating the presence of living G. stearothermophilus spores. If sterilization process was successful, indicator medium will remain purple after incubation.

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CD16 / Multi-variable Chemical Indicators, double card strips printed with reactive ink for Ethylene Oxide sterilization processes. Metals Free. Control of Ethylene Oxide (EO) sterilization processes. Conditions: 600 mg/l EO, RH 60%, 30 °C, 30 minutes // 600 mg/l EO, RH 60%, 54 °C, 20 minutes. Characteristics: Type 4 Chemical Indicator (according to ISO 11140-1). Double punched card strips printed with indicator ink. Specifications: Size: 200 x 15 mm. Initial Color: Purple/Brown. Final Color: Green. 100 % Toxic Heavy Metals free. Instructions For Use: Place a Chemdy® CD16 Multivariable Process Indicator within each package, bag or tray that will be sterilized by Ethylene Oxide. In rigid containers, place the indicator in every corner, or at least two diagonally opposite corners, to ensure mthat the sterilization agent has reached the most inaccessible areas. Perform the sterilization cycle. After the sterilization process has finished, remove the indicators from the sterilizer and analyze the results. For all the chemical indicators exposed to Ethylene Oxide, the ink must turn to the green reference color when the sterilization parameters are reached. More Info About This Product: Color Chart

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Multi-variable Chemical Indicator printed with reactive ink for Steam sterilization processes. Chemdye® CD29 Multivariable Process Indicators (Type 4 according to ISO 11140-1:2014 standard) are single-use chemical indicators that consist of one-side laminated punched paper double strips printed with indicator ink. These indicators have been designed to monitor Steam sterilization processes within loads, ensuring an adequate exposure to the sterilizing agent during the sterilization process and allowing to distinguish between processed and unprocessed items. Innovative highly sensitive yellow ink was developed to turn to dark brown/black when the indicator is exposed to Steam considering the critical process variables which provides additional quality assurance. Endpoint condition: 121 °C, 15 minutes; 134 °C, 3.5 minutes. Indicators 100 % free of toxic heavy metals. Instructions For Use: Place a Chemdye® CD29 Multivariable Process Indicator within each package, bag or tray that will be sterilized by Steam. In rigid containers, place the indicator in every corner, or at least two diagonally opposite corners, to ensure that the sterilization agent has reached the most inaccessible areas. Perform the sterilization cycle. After the sterilization process has finished, remove the indicators from the sterilizer and analyze the results. For all the chemical indicators exposed to Steam, the ink must turn to the dark brown/black reference color when the sterilization parameters are reached. For reference color, please refer to Result Reference Guide. Specifications: Process: Steam Initial Color: Yellow Final Color; Black Indicator Type: Type 4 chemical indicator Regulations: ISO 11140-1 More Info About This Product: Color Chart

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ICTP / Incubator Thermal Paper. Accessory for the IC10/20FR and IC10/20FRLCD incubator€™s thermal printer. Thermal Paper specially designed for using with Bionova® IC10/20FR, and Bionova® IC10/20FRLCD Auto-Reader€™s Printer. Specifications: Thermal Paper Roll. Color: white Paper length: 30 m. Paper width: 57 mm. Roll external diameter: 50 mm. Roll internal diameter: 13.4 mm. Its function is to record the final results of biological indicators subjected to sterilization process and quantitative analysis of hygiene monitoring systems at each activated position of IC10/20FR or IC10/20FRLCD, which allows registration into your sterilization record keeping book. Read IC10/20FR or IC10/20FRLCD directions for use, as appropriate.

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ICTP Mini / Thermal Paper specially designed for using with Bionova® Mini Bio, Bionova® Mini Pro Auto-Reader€™s Printer.Thermal Paper specially designed for using with Bionova® Mini Bio, Bionova® Mini Pro Auto-Reader€™s Printer. Specifications: Thermal Paper Roll. Color: White Paper Length: 4.7 m. Paper Width: 57 mm. Roll External Diameter: 23 mm. Roll Internal Diameter: 13.4 mm. Its function is to record the final results of biological indicators subjected to sterilization process and quantitative analysis of hygiene monitoring systems at each activated position of Bionova® Mini Bio and Mini Pro incubators, which allows record keeping in your sterilization records book. Read Bionova® Mini Bio and Mini Pro directions for use, as appropriate.

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McKesson Intravascular Catheters Made of soft, flexible radioopaque material. They are sterile, single-use and non-winged. The catheters are Not Made with Natural Rubber Latex, non-pyrogenic and DEHP-free. Size: 24G x 3/4". Packaged 50 to a box. WARNING: This product can expose you to bisphenol A (BPA), which is known to the State of California to cause birth defects or other reproductive harm. For more information, go to www.P65Warnings.ca.gov. Brand McKesson Manufacturer McKesson Brand Country of Origin South Korea Application Peripheral IV Catheter Catheter Length 0.75 Inch Catheter Material ETFE Color Code Yellow Gauge 24 Gauge Hub Material Plastic Hub Hub Type Straight Hub Needle Material Stainless Steel Number of Ports Without Port Port Type Without Port Product Dating McKesson Acceptable Dating: we will ship >= 90 days Safety Feature Without Safety Sterility Sterile UNSPSC Code 42221512 Usage Disposable X-Ray Compatibility Radiopaque

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Manufacturer # MS441A Brand McKesson Manufacturer McKesson Brand Country of Origin United States Application Dispensing Pin For Use With For Multi Dose Vials Specifications Small Packaging Box of 100

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McKesson 5-Liter Compact Concentrator with Oxygen Sensing Device 13.5 W x 24.5 H x 12 D inch 34% more compact than traditional 5-liter units. Exclusive OSD® (Oxygen Sensing Device) standard on every unit. Noticeably quiet operation. Recessed humidifier nook prevents damage. Turn-Down Technology: Below 2 1/2 LPM flow, the system automatically "turns down" its flow cycle resulting in 35% reduction in system pressure, reducing stress on compressor bearings and internal fittings. Also results in lower temperature (the lower heat of compression means longer cup seal life) and improved energy efficiency. Superior OSD®, faster sampling rate, increased accuracy and reliability, allows O2 check every 2 years. Weight: 36 lbs. WARNING: Cancer and Reproductive Harm www.P65Warnings.ca.gov Manufacturer # 146-525DS Brand McKesson Manufacturer McKesson Brand Country of Origin United States Application Oxygen Concentrator Dimensions 13-1/2 W X 12 D X 24-1/2 H Inch HCPCS E1390 Specifications With Oxygen Sensor, Pressure Relief Valve, 2-Prong Plug, 48 dBa Noise Level, Flame-Retardant Cabinet UNSPSC Code 42271702 Volume 5 Liter Weight 36 lbs. Latex Free Indicator Not Made with Natural Rubber Latex

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Manufacturer # MS721 Brand MedStream Manufacturer McKesson Brand Country of Origin China Administration Method Gravity Application Primary IV Administration Set Back Check Valve Without Back Check Valve Connection Type Male Luer Lock Connector DEHP Indicator DEHP-Free Tubing Drip Rate 20 Drops / mL Drip Rate Filter Without Filter Flow Control Type Roller Clamp / Slide Clamp Flow Regulator Without Flow Regulator Injection Port Type Grouping Standard Injection Port Material Polyvinyl Chloride (PVC) Number of Ports 1 Port Port Type Injection Y-Port Priming Volume 27.5 mL Priming Volume Spike Type Non-Vented Spike Sterility Sterile Tubing Length 81 Inch Tubing Tubing Length Range 73 to 96 Inches Tubing Type Standard Bore Tubing Type Solution UNSPSC Code 42221609

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McKesson Irrigation Tray Tray components packaged in the proper order for maximum efficiency and effectiveness. Piston syringe offers uninterrupted action in a single-hand technique. Disposable syringe with thumb ring is designed to minimize hand slippage and subsequent contamination of barrel or solution container. The barrel features raised, large and easy-to-read graduations, which are calibrated in both oz and cc. The elongated tip has an extra-large orifice for better removal of clots and mucous shreds. 60 cc sterile bulb syringe in graduated tray basin. Latex free and packaged sterile. Packaged: 20 Per Case McKesson # 911705 Manufacturer # 100122 Brand McKesson Manufacturer McKesson Brand Country of Origin China Application Irrigation Tray Contents 1 1 – 1000 cc Outer Tray, 1 - 60 mL Piston Syringe, 1 – Underpad, 18 x 13 Inch, 1 – Alcohol prep pad, 1 – 500c c plastic bottle, 1 – Tip protector HCPCS A4320 Sterility Sterile UNSPSC Code 42142612

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McKesson Intravascular Catheters Made of soft, flexible radioopaque material. They are sterile, single-use and non-winged. The catheters are Not Made with Natural Rubber Latex, non-pyrogenic and DEHP-free. Size: 20G x 1.25". Packaged 50 to a box. WARNING: This product can expose you to bisphenol A (BPA), which is known to the State of California to cause birth defects or other reproductive harm. For more information, go to www.P65Warnings.ca.gov.

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McKesson Cotton-Tipped Applicators Non-Sterile 3 inch (8 cm) Wood Shaft Single Use Not made with natural rubber latex. Packaged: 100 Per Bag, 10 Bags Per Box, 10 Boxes Per Case Manufacturer McKesson Brand Country of Origin China Application Swabstick FSA Eligible - Buy UOM Yes FSA Eligible - Sell UOM Yes HCPCS A4248 Number per Pack 100 per Pack Shaft Material Wood Shaft Sterility NonSterile Tip Material Cotton Tip UNSPSC Code 42141504 Latex Free Indicator Not Made with Natural Rubber Latex

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McKesson Tracheostomy Care Tray Sterile Single Use Contents: 1 - Pair Powder-Free Vinyl Gloves Cuffed, 1 - Tracheostomy Brush 5.25", 3 - Pipe Cleaners 5.5", 2 - Plastic Cotton Tipped Applicators 5", 1 - Tracheostomy Tie, 4 - Woven Gauze 4" x 4" (8-Ply), 1 - Woven Split Tracheostomy Sponge 4" x 4" (12-Ply), 1 - Towel 13" x 18" (2-Ply) EFFICIENCY AND VALUE - Our trays were designed with the help of medical staff to streamline components and reduce waste. CONVENIENCE AND STANDARDIZATION - Components are packaged in sequence of use, allowing the clinician to progress efficiently through procedures. Not made with natural rubber latex. Packaged: 20 Trays Per Case Manufacturer # 100126 Brand McKesson Manufacturer McKesson Brand Country of Origin China Application Tracheostomy Care Kit Contents 1 1 - Pair Powder-Free Vinyl Gloves Cuffed, 1 - Tracheostomy Brush 5.25", 3 - Pipe Cleaners 5.5", 2 - Plastic Cotton Tipped Applicators 5", 1 - Tracheostomy Tie, 4 - Woven Gauze 4" x 4" (8-Ply), 1 - Woven Split Tracheostomy Sponge 4" x 4" (12-Ply), 1 - Towel 13" x 18" (2-Ply) HCPCS A4629 Sterility Sterile UNSPSC Code 42271910 Latex Free Indicator Not Made with Natural Rubber Latex

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McKesson 14-Panel Drugs of Abuse Test All-in-one preliminary screening test for the qualitative detection of multiple drugs and drug metabolites in urine at specific cut-off levels CLIA-waved urine drug screen Offers panel size up to 14 analytes with an additional 3 adulteration tests Tests for Amphetamine, Barbiturates, Benzodiazepines, Buprenorphine, Cocaine, Methamphetamine, Ecstasy, Opiates, Methadone, Oxycodone, PCP, Propoxyphene, Tricyclic Antidepressants, and Marijuana at once Rapid, visually read results in just 5 minutes Of the 14 analytes, specifically, this test cup provides screening for Buprenorphine (BUP) and opiates (MOP300) at low-level cut offs Built-in specimen validity test (SVT) strip that verifies the validity of the specimen to compare with the Adulteration Color Comparison Chart Card (included) SVT strip provides a semi-quantitative screen for oxidants, specific gravity, and pH in human urine which can help to assess the integrity of the urine specimen Included dual-scale temperature strip helps monitor specimen tampering/validity No tipping, tilting or turning required Graduated to 4 oz (130 mL) Limited urine exposure; fits a variety of drug test settings Individually packaged in sealed foil pouch for added control For in vitro diagnostic use only Not Made with Natural Rubber Latex Packaged: 25 Per Box, 4 Boxes Per Case Manufacturer # 16-1145A3 Brand McKesson Manufacturer McKesson Brand Country of Origin China Application Drugs of Abuse Test Kit CLIA Classification CLIA Waived CLIA Classified CLIA Waived Contents 1 (25) Test Cups, (30) Pairs of Gloves, (5) Sheets of (5) Security Labels, Instruction Insert, Procedure Card, Adulteration Color Comparison Chart Card Number of Tests 25 Tests Product Dating McKesson Acceptable Dating: we will ship >= 180 days Purchase Program Type Standard Purchase Reading Type Visual Read Sample Type Urine Sample Specialty Toxicology Test Format Test Cup Format Test Kit Type Rapid Test Name AMP, BAR, BUP, BZO, COC, mAMP/MET, MDMA, MOP300, MTD, OXY, PCP, PPX, TCA, THC (OX, pH, SG) Test Type 14-Drug Panel with Adulterants Time to Results 5 Minute Results UNSPSC Code 41116146 Latex Free Indicator Not Made with Natural Rubber Latex

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McKesson 10-Panel Drugs of Abuse Test All-in-one preliminary screening test for the qualitative detection of multiple drugs and drug metabolites in urine at specific cut-off levels CLIA-waved urine drug screen Offers panel size up to 10 analytes with an additional 3 adulteration tests Tests for Amphetamine, Benzodiazepines, Buprenorphine, Cocaine, Methamphetamine, Ecstasy, Opiates, Methadone, Oxycodone, and Marijuana at once Rapid, visually read results in just 5 minutes Of the 10 analytes, specifically, this test cup provides screening for Buprenorphine (BUP) and opiates (MOP300) at low-level cut offs Built-in specimen validity test (SVT) strip that verifies the validity of the specimen to compare with the Adulteration Color Comparison Chart Card (included) SVT strip provides a semi-quantitative screen for oxidants, specific gravity, and pH in human urine which can help to assess the integrity of the urine specimen Included dual-scale temperature strip helps monitor specimen tampering/validity No tipping, tilting or turning required Graduated to 4 oz (130 mL) Limited urine exposure; fits a variety of drug test settings Individually packaged in sealed foil pouch for added control For in vitro diagnostic use only Not Made with Natural Rubber Latex Packaged: 25 Per Box, 4 Boxes Per Case Brand McKesson Manufacturer McKesson Brand Country of Origin China Application Drugs of Abuse Test Kit CLIA Classification CLIA Waived CLIA Classified CLIA Waived Contents 1 (25) Test Cups, (30) Pairs of Gloves, (5) Sheets of (5) Security Labels, Instruction Insert, Procedure Card, Adulteration Color Comparison Chart Card Number of Tests 25 Tests Product Dating McKesson Acceptable Dating: we will ship >= 180 days Purchase Program Type Standard Purchase Reading Type Visual Read Sample Type Urine Sample Specialty Toxicology Test Format Test Cup Format Test Kit Type Rapid Test Name AMP, BUP, BZO, COC, mAMP/MET, MDMA, MTD, MOP300, OXY, THC (OX, pH, SG) Test Type 10-Drug Panel with Adulterants Time to Results 5 Minute Results UNSPSC Code 41116146 Latex Free Indicator Not Made with Natural Rubber Latex

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McKesson 12-Panel Drugs of Abuse Test All-in-one preliminary screening test for the qualitative detection of multiple drugs and drug metabolites in urine at specific cut-off levels CLIA-waved urine drug screen Offers panel size up to 12 analytes with an additional 3 adulteration tests Tests for Amphetamine, Barbiturates, Benzodiazepines, Cocaine, Methamphetamine, Ecstasy Opiates, Methadone, Oxycodone, PCP, Tricyclic Antidepressants, and Marijuana at once Rapid, visually read results in just 5 minutes Of the 12 analytes, specifically, this test cup provides screening for opiates (MOP300) at low-level cut offs Built-in specimen validity test (SVT) strip that verifies the validity of the specimen to compare with the Adulteration Color Comparison Chart Card (included) SVT strip provides a semi-quantitative screen for oxidants, specific gravity, and pH in human urine which can help to assess the integrity of the urine specimen Included dual-scale temperature strip helps monitor specimen tampering/validity No tipping, tilting or turning required Graduated to 4 oz (130 mL) Limited urine exposure; fits a variety of drug test settings Individually packaged in sealed foil pouch for added control For in vitro diagnostic use only Not Made with Natural Rubber Latex Packaged: 25 Per Box, 4 Boxes Per Case Brand McKesson Manufacturer McKesson Brand Country of Origin China Application Drugs of Abuse Test Kit CLIA Classification CLIA Waived CLIA Classified CLIA Waived Contents 1 (25) Test Cups, (30) Pairs of Gloves, (5) Sheets of (5) Security Labels, Instruction Insert, Procedure Card, Adulteration Color Comparison Chart Card Number of Tests 25 Tests Product Dating McKesson Acceptable Dating: we will ship >= 180 days Purchase Program Type Standard Purchase Reading Type Visual Read Sample Type Urine Sample Specialty Toxicology Test Format Test Cup Format Test Kit Type Rapid Test Name AMP, BAR, BZO, COC, mAMP/MET, MDMA, MOP300, MTD, OXY, PCP, TCA, THC (OX, pH, SG) Test Type 12-Drug Panel with Adulterants Time to Results 5 Minute Results UNSPSC Code 41116146 Latex Free Indicator Not Made with Natural Rubber Latex

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McKesson Consult® 12-Panel Drugs of Abuse Test Dip Card Rapid, all-in-one screening test for the preliminary qualitative detection of multiple drugs and drug metabolites in urine at specific cutoff levels McKesson's Drugs of Abuse Test Dipcard offers panel size up to 12 analytes Drug panel includes amphetamines, barbiturates, benzodiazepines, cocaine, methamphetamine, morphine/opiates, methadone, oxycodone, phencyclidine, tricyclics, marijuana/hashish, and ecstasy (MDMA) Of the 12 analytes, specifically, this test dipcard provides screening for opiates at low-level cutoffs (MOP300) Adultreration test combined with DOA test strips Adulteration tests provide a semi-quantitative screen for oxidants, specific gravity, pH, nitrile, glutaraldehyde, and creatine in human urine which can help assess the integrity of the urine specimen Minimum detection time after suspected drug use is 2-7 hours CLIA-waived Results in 5 minutes For single use only Not Made with Natural Rubber Latex Packaged: 1 Per Pouch, 25 Pouches Per Box, 20 Boxes Per Case Manufacturer # 16-DTDC12P Brand McKesson Consult™ Manufacturer McKesson Brand Country of Origin China Application Drugs of Abuse Test Kit CLIA Classification CLIA Waived CLIA Classified CLIA Waived Number of Tests 25 Tests Product Dating McKesson Acceptable Dating: we will ship >= 180 days Purchase Program Type Standard Purchase Reading Type Visual Read Sample Type Urine Sample Specialty Toxicology Test Format Dip Card Format Test Kit Type Rapid Test Name AMP, BAR, BZO, COC, mAMP/MET, MDMA, MOP, MTD, OXY, PCP, TCA, THC Test Type 12-Drug Panel with Adulterants Time to Results 5 Minute Results UNSPSC Code 41116146

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McKesson 12-Panel Drugs of Abuse Test All-in-one preliminary screening test for the qualitative detection of multiple drugs and drug metabolites in urine at specific cut-off levels CLIA-waved urine drug screen Offers panel size up to 12 analytes with an additional 3 adulteration tests Tests for Amphetamine, Barbiturates, Buprenorphine, Cocaine, Methamphetamine, Ecstasy Opiates, Methadone, Oxycodone, PCP, and Marijuana at once Rapid, visually read results in just 5 minutes Of the 12 analytes, specifically, this test cup provides screening for Buprenorphine (BUP) and opiates (MOP300) at low-level cut offs Built-in specimen validity test (SVT) strip that verifies the validity of the specimen to compare with the Adulteration Color Comparison Chart Card (included) SVT strip provides a semi-quantitative screen for oxidants, specific gravity, and pH in human urine which can help to assess the integrity of the urine specimen Included dual-scale temperature strip helps monitor specimen tampering/validity No tipping, tilting or turning required Graduated to 4 oz (130 mL) Limited urine exposure; fits a variety of drug test settings Individually packaged in sealed foil pouch for added control For in vitro diagnostic use only Not Made with Natural Rubber Latex Packaged: 25 Per Box, 4 Boxes Per Case Manufacturer # 16-6125A3 Brand McKesson Manufacturer McKesson Brand Country of Origin China Application Drugs of Abuse Test Kit CLIA Classification CLIA Waived CLIA Classified CLIA Waived Contents 1 (25) Test Cups, (30) Pairs of Gloves, (5) Sheets of (5) Security Labels, Instruction Insert, Procedure Card, Adulteration Color Comparison Chart Card Number of Tests 25 Tests Product Dating McKesson Acceptable Dating: we will ship >= 180 days Purchase Program Type Standard Purchase Reading Type Visual Read Sample Type Urine Sample Specialty Toxicology Test Format Test Cup Format Test Kit Type Rapid Test Name AMP, BAR, BUP, BZO, COC, mAMP/MET, MDMA, MOP300, MTD, OXY, PCP, THC (OX, pH, SG) Test Type 12-Drug Panel with Adulterants Time to Results 5 Minute Results UNSPSC Code 41116146 Latex Free Indicator Not Made with Natural Rubber Latex

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McKesson Eye Wash Contains 98.3% purified water Cleanses the eye and helps relieve irritation or burning by removing loose foreign material Screw cap protected by a plastic tamper-evident seal Flush the affected eye as needed, controlling the rate of flow of the solution by applying pressure to the convenient squeeze bottle Sterile irrigiating solution great to have on hand for daily or emergency eye cleansing To avoid contamination, don’t touch the tip of the bottle to any surface Single use only Not Made with Natural Rubber Latex Packaged: 4 fl oz (118.3 mL) Per Bottle, 144 Bottles Per Case Manufacturer # MCK19818 Brand McKesson Manufacturer McKesson Brand Country of Origin Canada Application Eye Wash Solution Container Type Squeeze Bottle Contents 1 Active ingredient: 98.3% Purified Water Inactive ingredients: boric acid, sodium borate, sodium chloride FSA Eligible - Buy UOM Yes FSA Eligible - Primary UOM Yes FSA Eligible - Sell UOM Yes NDC Number 68599198104 Product Dating McKesson Acceptable Dating: we will ship >= 180 days UNSPSC Code 46181810 Volume 4 oz. Latex Free Indicator Not Made with Natural Rubber Latex

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McKesson Intermittent Catheter Tray With Red Rubber Catheter Sterile Single Use Contents: 1 - Red Rubber Catheter 14 FR, 1 - Pair of Vinyl Gloves, 1 - Specimen Container with Lid 4 oz., 1 - Fenestrated Drape 18 x 17 Inch, 1 - Pack of Three PVP Swabsticks, 1 - Pack of Lubricating Jelly 3 g, 1 - Underpad 18 x 17 Inch, 1 - Patient Label, 1 - Outer Tray 1000 mL. EFFICIENCY AND VALUE - Our trays were designed with the help of medical staff to streamline components and reduce waste. CONVENIENCE AND STANDARDIZATION - Components are packaged in sequence of use, allowing the clinician to progress efficiently through procedures. Packaged: 20 Trays Per Case Brand McKesson Manufacturer McKesson Brand Country of Origin China Application Intermittent Catheter Tray Collection Type 1000 mL Outer Tray Contents 1 1 - Outer Tray 1000 mL, 1 - Underpad 18 x 17 Inch, 1 - Fenestrated Drape 18 x 17 Inch, 1 - Pair of Vinyl Gloves Latex Free, 1 - Pack of Lubricating Jelly 3 g, 1 - Pack of Three PVP Swabsticks, 1 – 14Fr Red Rubber Catheter, 1 - Specimen Container with Lid 4 oz., 1 - Patient Label French Size 14 Fr. Material Red Rubber Securing Method Without Balloon Sterility Sterile Style Urethral UNSPSC Code 42142715 Latex Free Indicator Contains Latex

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McKesson Consult® 14-Panel Push-Button Drugs of Abuse Test Cup Rapid, all-in-one screening test for the preliminary qualitative detection of multiple drugs and drug metabolites in urine at specific cutoff levels Test cup offers panel size up to 14 analytes with an additional 3 adulteration tests Drug panel includes amphetamines, barbiturates, buprenorphine/norbuprenorphine, benzodiazepine, cocaine, methamphetamine, morphine/opiates (2000 ng/ml), morphine/opiates (300 ng/ml ), methadone, oxycodone, phencyclidine, tricyclics, marijuana/hashish, and ecstasy (MDMA) Built-in specimen validity tests (SVT) Adulterant test strip provides a semi-quantitative screen for oxidants, specific gravity, and pH in human urine to assess the integrity of the urine specimen Dual-scale temperature strip included to help monitor specimen tampering and validity Delivers rapid results in 5 to 7 minutes No tipping, tilting or turning required CLIA-waived Equilibrate refrigerated specimens and devices to room temperature before performing the test For single use only Not Made with Natural Rubber Latex Packaged: 1 Per Pouch, 25 Pouches Per Box Manufacturer # MCK03-4490 Brand McKesson Consult™ Manufacturer McKesson Brand Country of Origin United States Application Drugs of Abuse Test Kit CLIA Classification CLIA Waived CLIA Classified CLIA Waived Number of Tests 25 Tests Product Dating McKesson Acceptable Dating: we will ship >= 180 days Purchase Program Type Standard Purchase Reading Type Visual Read Sample Type Urine Sample Specialty Toxicology Test Format Test Cup Format Test Kit Type Rapid Test Name AMP, BAR, BUP, BZD, COC, MET, MOR, MOR300, MTD, OXY, PCP, TCA, THC, XTC Test Type 14-Drug Panel Time to Results 5 to 7 Minute Results UNSPSC Code 41116146 Latex Free Indicator Not Made with Natural Rubber Latex

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McKesson Hand Pump Designed for McKesson Brand Antiseptic Skin Cleaner 16-CHGGL Manufacturer # 29901-016 Brand McKesson Manufacturer McKesson Brand Country of Origin United States Application Hand Pump For Use With For Use with McKesson Brand Antiseptic Skin Cleaner 16-CHGGL UNSPSC Code 53131651

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McKesson I.V. Start Kit with PVP Prep Pad, PVP Ointment Sterile Single Use Contents: 1 - Tourniquet, 1 - PVP Prep Pad (Non-Sterile), 1 - Alcohol Prep Pad, 1 - PVP Ointment, 1 g (Non-Sterile), 2 - Woven Gauze 2" x 2" (8-Ply), 1 - Transparent Dressing, 2.37" x 2.75", 1 Roll of Tape, 1 - Patient Label EFFICIENCY AND VALUE - Our trays were designed with the help of medical staff to streamline components and reduce waste. CONVENIENCE AND STANDARDIZATION - Components are packaged in sequence of use, allowing the clinician to progress efficiently through procedures. Not made with natural rubber latex. Packaged: 50 Kits Per Case Manufacturer # 100123 Brand McKesson Manufacturer McKesson Brand Country of Origin China Application IV Start Kit Contents 1 1 - Tourniquet 1 - PVP Prep Pad (Non-Sterile) 1 - Alcohol Prep Pad 1 - PVP Ointment (Non-Sterile)1 gram 2 - Woven Gauze 2 x 2 Inch (8-Ply) 1 - Transparent Dressing, 2.37 x 2.75Inch 1 Roll of Tape 1 - Patient Label Sterility Sterile UNSPSC Code 42221507

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McKesson I.V. Start Kit with Tegaderm™ Dressing, PVP Swabstick Sterile Single Use Contents: 1 - Tourniquet, 1 - PVP Swabstick, 1 - Alcohol Prep Pad, 2 - Woven Gauze 2" x 2" (8-Ply), 2 - Tape Strips .5" x 4", 2 - Tape Strips 1" x 4" , 1 - Tegaderm™ Dressing, 2.37" x 2.75", 1 - IV Change Label EFFICIENCY AND VALUE - Our trays were designed with the help of medical staff to streamline components and reduce waste. CONVENIENCE AND STANDARDIZATION - Components are packaged in sequence of use, allowing the clinician to progress efficiently through procedures. Not made with natural rubber latex. Packaged: 50 Kits Per Case Tegaderm™ is a trademark of 3M Manufacturer # 25-8825 Brand McKesson Manufacturer McKesson Brand Country of Origin China Application IV Start Kit Contents 1 1 - Tourniquet 1 - PVP Swabstick 1 - Alcohol Prep Pad 2 - Woven Gauze 2 x 2 Inch(8-Ply) 2 - Tape Strips 0.5 x 4 Inch 2 - Tape Strips 1 x 4 Inch 1 - Tegaderm™ Dressing, 2.37 x 2.75 1 - IV Change Label Sterility Sterile UNSPSC Code 42221507 Latex Free Indicator Not Made with Natural Rubber Latex

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McKesson I.V. Start Kit with Tegaderm™ Dressing, PVP Prep Ampule Sterile Single Use Contents: 1 - Tourniquet, 1 - PVP Prep Ampule, 1 - Alcohol Prep Pad, 2 - Non- Woven Gauze, 2" x 2" (4Ply), 1 - Tegaderm™ Dressing 2.37" x 2.75", 1 - Roll of Transpore™ Tape EFFICIENCY AND VALUE - Our trays were designed with the help of medical staff to streamline components and reduce waste. CONVENIENCE AND STANDARDIZATION - Components are packaged in sequence of use, allowing the clinician to progress efficiently through procedures. Not made with natural rubber latex. Packaged: 50 Kits Per Case Tegaderm™ and Transpore™ are trademarks of 3M. Manufacturer # 25-5840 Brand McKesson Manufacturer McKesson Brand Country of Origin China Application IV Start Kit Contents 1 1 - Tourniquet 1 - PVP Prep Ampule 1 - Alcohol Prep Pad 2 - Non- Woven Gauze, 2 x 2 Inch (4Ply) 1 - Tegaderm™ Dressing 2.37 x 2.75 Inch 1 - Roll of Transpore™ Tape Sterility Sterile UNSPSC Code 42221507 Latex Free Indicator Not Made with Natural Rubber Latex

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McKesson I.V. Start Kit with Tegaderm™ Dressing, Prevantics® Antiseptic Swab Pad Sterile Single Use Contents: 1 - Tourniquet, 1 - Prevantics® Antiseptic Swab Pad, 2 - Non-Woven Gauze 2 x 2 Inch (4-Ply), 1 - Tegaderm™ Dressing 2.37 x 2.75 Inch, 1 - Roll of Transpore™ Tape, 1 - IV Change Label EFFICIENCY AND VALUE - Our trays were designed with the help of medical staff to streamline components and reduce waste. CONVENIENCE AND STANDARDIZATION - Components are packaged in sequence of use, allowing the clinician to progress efficiently through procedures. Not made with natural rubber latex. Packaged: 100 Kits Per Case Prevantics® is a registered trademark of PDI Products. Tegaderm™ and Transpore™ are trademarks of 3M. Manufacturer # 25-57931 Brand McKesson Manufacturer McKesson Brand Country of Origin China Application IV Start Kit Contents 1 1 - Tourniquet 1 - Prevantics® Antiseptic Swab Pad 2 - Non-Woven Gauze 2 x 2 Inch (4-Ply) 1 - Tegaderm™ Dressing 2.37 x 2.75 Inch 1 - Roll of Transpore™ Tape 1 - IV Change Label Sterility Sterile UNSPSC Code 42221507 Latex Free Indicator Not Made with Natural Rubber Latex

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McKesson Steam Sterilization Integrator For placement inside packs prior to processing, this integrator moves from left to right when all parameters for sterilization have been met. Class 5 integrator provides immediate readout for monitoring the Steam sterilization process. For use with all Steam processes (gravity, pre-vacuum or flash). Not made with natural rubber latex. Packaged: 1000 Integrators Per Pack Brand McKesson Manufacturer McKesson Brand Country of Origin United States Application Sterilization Chemical Integrator Strip Class Class 5 Indicator Change Color Bar Is_ECAT N Is_GSA N Is_VA Y Length 4 Inch Sterilization Compatibility Steam Time to Results All Processing Times UNSPSC Code 42281803 Latex Free Indicator Not Made with Natural Rubber Latex

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McKesson I.V. Start Kit with Tegaderm™ Dressing, PVP Prep Pad Sterile Single Use Contents: 1 - Tourniquet, 1 - PVP Prep Pad, 1 - Alcohol Prep Pad, 2 - Non- Woven Gauze, 2" x 2" (4Ply), 1 - Tegaderm™ Dressing 2.62" x 2.75", 1 - Roll of Transpore™ Tape EFFICIENCY AND VALUE - Our trays were designed with the help of medical staff to streamline components and reduce waste. CONVENIENCE AND STANDARDIZATION - Components are packaged in sequence of use, allowing the clinician to progress efficiently through procedures. Not made with natural rubber latex. Packaged: 50 Kits Per Case Tegaderm™ and Transpore™ are trademarks of 3M. Manufacturer # 25-5890 Brand McKesson Manufacturer McKesson Brand Country of Origin China Application IV Start Kit Contents 1 1 - Tourniquet 1 - PVP Prep Pad 1 - Alcohol Prep Pad 2 - Non- Woven Gauze 2 x 2 Inch(4Ply) 1 - Tegaderm™ Dressing 2.62 x 2.75 Inch 1 - Roll of Transpore™ Tape Sterility Sterile UNSPSC Code 42221507 Latex Free Indicator Not Made with Natural Rubber Latex

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Brand Angiocath™ Manufacturer BD Country of Origin Brazil Application Peripheral IV Catheter Catheter Length 1 Inch Catheter Material FEP Polymer Color Code Blue Flow Rate 28 mL / min Gauge 22 Gauge Hub Material Plastic Hub Hub Type Straight Hub Needle Material Stainless Steel Number of Ports Without Port Port Type Without Port Product Dating McKesson Acceptable Dating: we will ship >= 90 days Safety Feature Without Safety Tubing Diameter 0.546 - 0.648 mm ID UNSPSC Code 42221512 X-Ray Compatibility Radiopaque

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Features McKesson Steam Sterilization Integrator For placement inside packs prior to processing, this integrator moves from left to right when all parameters for sterilization have been met. Class 5 integrator provides immediate readout for monitoring the Steam sterilization process. For use with all Steam processes (gravity, pre-vacuum or flash). Not made with natural rubber latex. Packaged: 100 Integrators Per Pack, 10 Packs Per Case Brand McKesson Manufacturer McKesson Brand Country of Origin United States Application Sterilization Chemical Integrator Strip Class Class 5 Indicator Change Color Bar Is_ECAT N Is_GSA N Is_VA Y Length 4 Inch Sterilization Compatibility Steam Time to Results All Processing Times UNSPSC Code 42281806 Latex Free Indicator Not Made with Natural Rubber Latex

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McKesson Prevent® R Shielded IV Catheters Push-button safety design allows one-handed needle retraction into the safety shield for reduced risk of accidental needle-stick injuries Straight hub and contoured finger grip for comfortable and simple catheter insertion Yellow, ISO-compliant, color-coded catheter hub and packaging for easy size identification of 24-gauge needle Flash chamber provides visual confirmation that catheter has entered the vein Enhanced flashback design features notched needle to provide optimal visualization of blood return along the needle shaft allowing administrator immediate confirmation of vessel entry Soft, flexible, kink-resistant material further softens inside to conform to the shape of the vessel Radiopaque materials allow use during x-rays or other form of radiation Individually wrapped, disposable catheters - featuring a needle sheath - designed for single sterile use Non-pyrogenic, DEHP-free, and not made with natural rubber latex Packaged: 1 Per Pack, 50 Packs Per Box, 4 Boxes Per Case Brand McKesson Prevent® R Manufacturer McKesson Brand Country of Origin United States Alternate Manufacturer Number 192-PB2475 Application Peripheral IV Catheter Catheter Length 0.75 Inch Color Code Yellow Flow Rate 20 mL / min Gauge 24 Gauge Hub Material Plastic Hub Needle Material Stainless Steel Needle Point Style Notched Needle Number of Ports Without Port Port Type Without Port Safety Feature Button Retracting Safety Needle Sterility Sterile Tubing Diameter 0.521 mm ID UNSPSC Code 42221512 Usage Disposable X-Ray Compatibility Radiopaque Latex Free Indicator Not Made with Natural Rubber Latex

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McKesson Prevent® R Shielded IV Catheters Push-button safety design allows one-handed needle retraction into the safety shield for reduced risk of accidental needle-stick injuries Featured stabilizing wings provide a large surface area for easier application of tape or other catheter securement device Pink, ISO-compliant, color-coded catheter hub and packaging for easy size identification of 20-gauge needle Flash chamber provides visual confirmation that catheter has entered the vein Enhanced flashback design features notched needle to provide optimal visualization of blood return along the needle shaft allowing administrator immediate confirmation of vessel entry Soft, flexible, kink-resistant material further softens inside to conform to the shape of the vessel Radiopaque materials allow use during x-rays or other form of radiation High pressure design suitable for use with power injectors rated for a maximum of 300 psi Individually wrapped, disposable catheters - featuring a needle sheath - designed for single sterile use Non-pyrogenic, DEHP-free, and not made with natural rubber latex Packaged: 1 Per Pack, 50 Packs Per Box, 4 Boxes Per Case Brand McKesson Prevent® R Manufacturer McKesson Brand Country of Origin United States Alternate Manufacturer Number 192-PB201W Application Peripheral IV Catheter Catheter Length 1 Inch Color Code Pink Flow Rate 65 mL / min Gauge 20 Gauge Hub Material Plastic Hub Needle Material Stainless Steel Needle Point Style Notched Needle Number of Ports Without Port Port Type Without Port Pressure Rating 300 psi Safety Feature Button Retracting Safety Needle Sterility Sterile Tubing Diameter 0.800 mm ID UNSPSC Code 42221512 Usage Disposable X-Ray Compatibility Radiopaque Latex Free Indicator Not Made with Natural Rubber Latex

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Features McKesson Prevent® R Shielded IV Catheters Push-button safety design allows one-handed needle retraction into the safety shield for reduced risk of accidental needle-stick injuries Straight hub and contoured finger grip for comfortable+AX17 and simple catheter insertion Blue, ISO-compliant, color-coded catheter hub and packaging for easy size identification of 22-gauge needle Flash chamber provides visual confirmation that catheter has entered the vein Enhanced flashback design features notched needle to provide optimal visualization of blood return along the needle shaft allowing administrator immediate confirmation of vessel entry Soft, flexible, kink-resistant material further softens inside to conform to the shape of the vessel Radiopaque materials allow use during x-rays or other form of radiation High pressure design suitable for use with power injectors rated for a maximum of 300 psi Individually wrapped, disposable catheters - featuring a needle sheath - designed for single sterile use Non-pyrogenic, DEHP-free, and not made with natural rubber latex Packaged: 1 Per Pack, 50 Packs Per Box, 4 Boxes Per Case Manufacturer McKesson Brand Country of Origin United States Alternate Manufacturer Number 192-PB221 Application Peripheral IV Catheter Catheter Length 1 Inch Color Code Blue Flow Rate 35 mL / min Gauge 22 Gauge Hub Material Plastic Hub Hub Type Straight Hub Needle Material Stainless Steel Needle Point Style Notched Needle Number of Ports Without Port Port Type Without Port Pressure Rating 300 psi Safety Feature Button Retracting Safety Needle Sterility Sterile Tubing Diameter 0.648 mm ID UNSPSC Code 42221512 Usage Disposable X-Ray Compatibility Radiopaque Latex Free Indicator Not Made with Natural Rubber Latex

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McKesson Prevent® Biohazard Infectious Waste Sharps Container Red Capacity: 1 Quart Dimensions: 6.25H x 4.25W x 4.25D Inch Puncture Resistant - Strong polypropylene containers meet or exceed industry standards. Maximum Container Volume - Horizontal drops allow full utilization of capacity to the fill-line. Stackable - Convenient, economical shipping and storage. Translucent Lid - Quick visual identification of fill level. Locking Lid - Ensures safe transport. Do not reuse. Not made with natural rubber latex. Packaged: 80 Per Case Manufacturer McKesson Brand Country of Origin Unknown Application Sharps Container Base Color Red Base Dimensions 6-1/4 H X 4-1/4 W X 4-1/4 D Inch Is_ECAT N Is_GSA N Is_VA Y Lid Color Translucent Lid Lid Style Vertical Entry Locking Type Locking Lid Material Polypropylene PG-II Rated Not PG-II Rated Placement Free Standing Sterility NonSterile Style Phlebotomy UNSPSC Code 42192802 Volume 0.25 Gallon Volume Range Under 0.5 Gallon Latex Free Indicator Not Made with Natural Rubber Latex

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