Medical Device Cleaning and disinfection Validation

We validate your medical device cleaning or disinfection instructions, as detailed in your IFU, which can be manual or automated.

We offer testing services to ensure the cleaning and disinfection instructions outlined in your Instructions for Use (IFU) have been fully validate. As outlined in the ISO 17664 Processing of health care products: Information to be provided by the medical device manufacturer for the processing of medical devices
(part 1 Critical and semi-critical medical devices, and part 2 Non-critical medical devices), all Medical Devices manufactures are responsible to provide instruction of use when reprocessing of the device is intended. These instruction shall be fully validated to ensure safety of the device. Both manual and automated (Washer disinfector) processes shall be validated as per ISO 17664.

Medical Device Cleaning – Everything You Need to Know

In order to gauge the most accurate representation of the cleaning procedure, the validation experiments require the test device t...

Cleaning validation with ATP : Everything You Need to Know

Post-cleaning, any residual ATP is collected from the sample and measured using the ATP bioluminescence monitor

FDA Validation Requirements for Reusable Medical Devices: 21 CFR 801.5

FDA Validation Requirements for Reusable Medical Devices: guidance on the requirements and criteria for validation data