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Non-Active Medical Devices


TÜV Rheinland

In a medical setting, it is not only the high-tech equipment that makes a difference to positive outcomes. Non-active medical devices also have a crucial role to play and are held to equally high standards when it comes to safety and compliance. As a manufacturer of non-active medical equipment, you strive to fulfill the expectations of health care professionals as well as the authorities in charge of regulating your products. Our services can help you meet these expectations. With experts in the field active around the globe, we enable you to demonstrate the safety and reliability of the devices you manufacture, and at the same time to inspire confidence in your customers.

Our portfolio

Active Implantable Medical Devices (AIMD)
Active Implantable Medical Devices (AIMD)  

Conformity Assessments for Your Active Implants.

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

Active and Non-Active Medical Devices.

EN ISO 13485 Certification
Certification According to EN ISO 13485 

Validating Your Quality Management System.

Green Product Mark
Green Product Mark 

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

In-Vitro Diagnostic Devices (IVD)
In-vitro-Diagnostic (IVD)  

We Can Test and Certify Your Quality Management System and Products.

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!