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Reprocessing of Medical Devices


TÜV Rheinland

For quality patient care, adequately reprocessing medical devices is a crucial step. Manufacturers of medical equipment intended for reprocessing must be aware of the challenges associated with reuse starting at the design phase and continuing through testing, packaging and the implementation of safety measures. Objective, reliable third-party input is invaluable throughout this process, and our services provide this necessary feedback from experienced specialists using state-of-the-art laboratory facilities. We enable you to demonstrate the safety and functionality of your products for regulatory authorities and customers alike.

Our portfolio

Active und Non-Active Medical Devices
Active and Non-Active Medical Devices 

Active and Non-Active Medical Devices.

Green Product Mark
Green Product Mark 

One, single label indicating the overall environmental preferability of your product - direct, quick and efficient.

Japanese Pharmaceutical Affairs Law (PAL)
Japanese Pharmaceutical Affairs Law (PAL) 

Is Your Medical Equipment Certified in Japan?

Contact

Get in contact with us!

Get in contact with us!