9095.11.752
Ref 9095.11.752Model General Instrument - Torque Wrench Zimmer Connection 5Nm
9095.11.752 is a Class I device made by Limacorporate, registered in EUDAMED on 6 Nov 2026 (Basic UDI-DI B-08033390109499) and listed in FDA GUDID since 8 Sep 2022 (UDI-DI 08033390109499), active as of 7 Nov 2026.
Active
CE MDD
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/MDD EUDAMED | NumberB-08033390109499 08033390109499 | Date6 Nov 2026 | StatusActive |
| United States | GUDID listing GUDID | Number08033390109499 | Date8 Sep 2022 | StatusListed |
Official records
- EUDAMED public site B-08033390109499
- AccessGUDID record 08033390109499
Across registries
- EUDAMED Basic UDI-DI B-08033390109499 registered 6 Nov 2026 Active
- FDA GUDID UDI-DI 08033390109499 listed 8 Sep 2022 Listed
Timeline
- Listed FDA GUDID 08033390109499
- Registered EUDAMED B-08033390109499
Coverage
- Active
- Expiring
- Withdrawn
- Listed
- Not covered
- European Union
- United States
Specification
- Trade name
- General Instrument - Torque Wrench Zimmer Connection 5Nm
- Generic name
- Surgical torque wrench, reusable
- Model / Ref / Catalog
- 9095.11.752, General Instrument - Torque Wrench Zimmer Connection 5Nm
- Primary DI / UDI-DI
- 08033390109499
- Basic UDI-DI
- B-08033390109499
- FDA product code
- HRW
- EMDN code
- L0999 Orthopaedic and traumatological surgery instruments, reusable - other
- GMDN term
- Surgical torque wrench, reusable
- Device class
- Class I
- Regulation number
- 888.1250
- EU registration type
- Legacy device (under a directive)
- EU market of registration
- Italy
- GUDID distribution status
- In Commercial Distribution
- Sterilisation method
- Moist Heat or Steam Sterilization
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