398.986
by Synthes
398.986 (398986) is a Class I device made by Synthes, listed in FDA GUDID since 13 Oct 2017 (UDI-DI 10887587041827), registry data as of 23 Oct 2026.
Listed
Valid until
Not applicable
FDA recalls
Not checked
Documents
None
Trust
Regulatory status
| Region | Authorization | Number | Date | Status |
|---|---|---|---|---|
| United States | GUDID listing | Number10887587041827 | Date13 Oct 2017 | StatusListed |
Official records
- AccessGUDID record 10887587041827
Coverage
- Active
- Expiring
- Withdrawn
- Listed
- Not covered
United States — GUDID listing Listed
Specification
- Generic name
- Bone holding forceps
- Model / Ref / Catalog
- 398.986, 398986
- Primary DI / UDI-DI
- 10887587041827
- FDA product code
- HTD
- GMDN term
- Bone holding forceps
- Device class
- Class I
- Regulation number
- 878.4800
- GUDID distribution status
- In Commercial Distribution
- Sterilisation method
- Moist Heat or Steam Sterilization
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