Identity™ SBRV9002
by Zimmer, Inc.
Ref SBRV9002
Identity™ SBRV9002 is a Class I device made by Zimmer, Inc., registered in EUDAMED on 20 Oct 2026 (Basic UDI-DI 889024BQT3J) and listed in FDA GUDID since 22 Sep 2022 (UDI-DI 00889024627918), active as of 22 Oct 2026.
Active
CE MDR
Valid until
No date given
FDA recalls
Not checked
Documents
None linked in EUDAMED
Trust
Regulatory status
| Region | Authorization | Number | Date | Status |
|---|---|---|---|---|
| European Union | CE/MDR EUDAMED | Number889024BQT3J 00889024627918 | Date20 Oct 2026 | StatusActive |
| United States | GUDID listing GUDID | Number00889024627918 | Date22 Sep 2022 | StatusListed |
Official records
- EUDAMED public site 889024BQT3J
- AccessGUDID record 00889024627918
Across registries
- EUDAMED Basic UDI-DI 889024BQT3J registered 20 Oct 2026 Active
- FDA GUDID UDI-DI 00889024627918 listed 22 Sep 2022 Listed
Timeline
- Listed FDA GUDID 00889024627918
- Registered EUDAMED 889024BQT3J
Coverage
- Active
- Expiring
- Withdrawn
- Listed
- Not covered
- European Union
- United States
Specification
- Trade name
- Identity™
- Generic name
- Orthopaedic inorganic implant inserter/extractor, reusable
- Device name
- IDENTITY Hum Adapter Remover Sleeve
- Model / Ref / Catalog
- SBRV9002
- Primary DI / UDI-DI
- 00889024627918
- Basic UDI-DI
- 889024BQT3J
- FDA product code
- HWB
- EMDN code
- L091001 Instruments for insertion and extraction of materials for osteosynthesis, reusable
- GMDN term
- Orthopaedic inorganic implant inserter/extractor, reusable
- Device class
- Class I
- Regulation number
- 888.4540
- EU registration type
- Standard device
- EU market of registration
- Netherlands
- GUDID distribution status
- In Commercial Distribution
- Sterilisation method
- Moist Heat or Steam Sterilization
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