General Instruments CI-11438-03
General Instruments CI-11438-03 is a Class I device made by Alphatec Spine, Inc., listed in FDA GUDID since 12 Nov 2023 (UDI-DI 00840180522547), 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 | Number00840180522547 | Date12 Nov 2023 | StatusListed |
Official records
- AccessGUDID record 00840180522547
Coverage
- Active
- Expiring
- Withdrawn
- Listed
- Not covered
United States — GUDID listing Listed
Specification
- Trade name
- General Instruments
- Generic name
- Bone cutter
- Model / reference
- CI-11438-03
- Primary DI / UDI-DI
- 00840180522547
- 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
Similar devices
Other devices filed under FDA product code HTZ (INSTRUMENT, CUTTING, ORTHOPEDIC).
- CODMAN SUCTION PUNCH-PRODUCT CODES by Codman & Shurtleff, Inc.
- ROSETTE KNIFE 4MM by Stainless Mfg., Inc.
- Wire cutter 100.11.115 by Zimmer, Inc.
- Gimmi CA.1152.28 by Gimmi GmbH
- Gimmi CA.1153.34 by Gimmi GmbH
- RETROGRADE KNIFE 4MM & 5MM by Stainless Mfg., Inc.
- GUILLOTINE BLADE by Ortho Pared Instruments, Inc.
- ARTHROSCOPY SUCTION BIOPSY PUNCH by T. Korossurgical Instruments Corp.
- KOGAN ENDOSPECULUM 9-1/2 by J. Sklar Mfg. Co., Inc.
- Newclip Instruments ANC1105 by NEWCLIP TECHNICS