This standard covers standard practices for the biological evaluation of the safety of medical devices used indentistry. In addition, this document covers biological evaluation of the device component of combinationproducts, including those with a pharmacological agent or biologic component as an integral part of thedevice.
This standard does not cover testing of materials and devices that do not come into direct or indirect contactwith the patient’s body.
- Published:
- 12/23/2015
- ANSI:
- ANSI Approved
- Number of Pages:
- 45
- File Size:
- 1 file , 1.1 MB
- Redline File Size:
- 2files, 6.2 MB
- Note:
- This product is unavailable in Ukraine, Russia, Belarus
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