Reusable Medical Device Cleaning Validations
Nelson Laboratories offers a full range of medical device cleaning validation services to validate manufacturers’ cleaning instructions for reusable devices. This includes contamination, cleaning and post-reprocessing effectiveness evaluations. Simulated-use testing practices are employed to simulate actual surgical procedures rather than direct inoculation methods. Options are available to use validated or customized test soils to create clinically relevant conditions. This test complies with AAMI TIR 12, AAMI TIR 30 and the FDA draft guidance document for processing/reprocessing medical devices in health care settings. The reprocessing scientists at Nelson Laboratories actively serve on applicable AAMI committees and have expertise in creating appropriate worst-case testing conditions to help device manufacturers meet regulatory expectations.
- AAMI TIR 12
- AAMI TIR 30
Standard turn around times (TAT) are listed below. Ask an expert for a specific consultation on your product. If you are ready to submit your samples for testing, click here to fill out the Sample Submission Form.
|Code||Test||TAT (days)||Request Quote|
|RVC110||Device Cleaning Validation for Reuse or Reprocessing||Add|
RVC110 - Device Cleaning Validation for Reuse or Reprocessing
Standard TAT not available for this product
Cleaning validations evaluate the recommended cleaning procedure for a reusable device according to AAMI TIR12and AAMI TIR30. This information is needed to assure that once the device has been used, it can be properly cleaned. It is the responsibility of the manufacturer to apply this data, along with their own functionality and sterilization data, to the instructions for the end user.
Contamination: The devices are contaminated with organic material that may contain Escherichia coli, Geobacillus stearothermophilus, Staphylococcus aureus, or other appropriate microorganisms, along with other clinically relevant markers such as protein, hemoglobin, carbohydrates, total organic carbon and endotoxin. The device’s intended use and wait time between patient use and cleaning are considered in determining the contamination method. The devices are often sprayed, handled with soiled gloves and/or immersed in the test soil. All movable parts may be actuated to simulate clinical use and then left in contact with the soil for an appropriate time. The devices are removed from the soil and allowed to set for an appropriate time to simulate the wait time between use and reprocessing.
Positive device recovery: Extraction(s) will be performed to determine the number of viable organisms and/or additional markers on a positive device. Multiple extractions are often performed to obtain an extraction efficiency, a determination of how well organism(s) and marker(s) are recovered using the extraction method selected.
Cleaning process: The test devices will be cleaned using the recommended cleaning procedure from the manufacturer. A manual process might involve immersing devices in detergent prepared according to the detergent manufacturer’s recommendations. A soft bristled brush may be used to aid in soil removal, paying particular attention to crevices and hard-to-clean areas. Some devices may need to be subjected to a mechanical step that may include ultrasonic cleaning in an enzymatic detergent. Nelson Laboratories is also capable of performing fully automated validations in common healthcare washer/disinfectors.
Residual testing: After the devices are cleaned, they are extracted using a validated method to remove any remaining soil. The extraction fluid is then tested to evaluate bioload reduction and/or residual amounts of test markers remaining on the device. This testing combined with visual inspection help to validate that the process was appropriate to adequately clean the device.