General Instruments CI-10167-12
General Instruments CI-10167-12 is a Class I device made by Alphatec Spine, Inc., listed in FDA GUDID since 19 Sep 2020 (UDI-DI 00811801032929), registry data as of 22 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 | Number00811801032929 | Date19 Sep 2020 | StatusListed |
Official records
- AccessGUDID record 00811801032929
Coverage
- Active
- Expiring
- Withdrawn
- Listed
- Not covered
United States — GUDID listing Listed
Specification
- Trade name
- General Instruments
- Generic name
- Bone cutter
- Model / reference
- CI-10167-12
- Primary DI / UDI-DI
- 00811801032929
- FDA product code
- HTZ
- GMDN term
- Bone cutter
- 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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