357.97
by Synthes GmbH
357.97 (35797) is a Class I device made by Synthes GmbH, listed in FDA GUDID since 20 Feb 2017 (UDI-DI 10886982196712), registry data as of 12 Nov 2026.
Listed
Valid until
Not applicable
FDA recalls
Not checked
Documents
None
Trust
Regulatory status
| Region | Authorization | Number | Date | Status |
|---|---|---|---|---|
| United States | GUDID listing | Number10886982196712 | Date20 Feb 2017 | StatusListed |
Official records
- AccessGUDID record 10886982196712
Coverage
- Active
- Expiring
- Withdrawn
- Listed
- Not covered
United States — GUDID listing Listed
Specification
- Generic name
- Bone nail trial, reusable
- Model / Ref / Catalog
- 357.97, 35797
- Primary DI / UDI-DI
- 10886982196712
- FDA product code
- FZX
- GMDN term
- Bone nail trial, reusable
- 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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