The biocompability of medical device is the basic requirement to ensure safety of medical devices. Biocompatibility testing shall be conducted in compliance with Principles of Good Laboratory Practice (GLP) and/or ISO/IEC 17025. Before any test, check related administration if test results of the third-party is accepted.
Some third parties which can carry out biocompatibility testing according to ISO 10993 are listed as below:
- TUV-SUD.
- UL.
- Toxikon.
- Pacific Biolabs.
- Nelson Labs.
- American Preclinical Services.
- Cytox.
- NAMSA
- Medical Engineering Technologies Ltd.
- Shanghai Biomaterial Research and Test Center, cerificated by CFDA.
- WuXi Apptec, cerificated by CFDA.
- GLR Labs.
- RCC Labs.
- PWG.
