S.0598.95
by Gimmi GmbH
Ref S.0598.95
S.0598.95 is a Class I device made by Gimmi GmbH, registered in EUDAMED on 8 Sep 2026 (Basic UDI-DI B-04049047087632) and listed in FDA GUDID since 3 May 2023 (UDI-DI 04049047087632), active as of 23 Oct 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-04049047087632 04049047087632 | Date8 Sep 2026 | StatusActive |
| United States | GUDID listing GUDID | Number04049047087632 | Date3 May 2023 | StatusListed |
Official records
- EUDAMED public site B-04049047087632
- AccessGUDID record 04049047087632
Across registries
- EUDAMED Basic UDI-DI B-04049047087632 registered 8 Sep 2026 Active
- FDA GUDID UDI-DI 04049047087632 listed 3 May 2023 Listed
Timeline
- Listed FDA GUDID 04049047087632
- Registered EUDAMED B-04049047087632
Coverage
- Active
- Expiring
- Withdrawn
- Listed
- Not covered
- European Union
- United States
Specification
- Generic name
- Soft-tissue surgical hook, reusable
- Model / reference
- S.0598.95
- Description
- HOOK FOR HERNIA MESH; Ø 2.8 MM; WORKING LENGTH 300 MM
- Primary DI / UDI-DI
- 04049047087632
- Basic UDI-DI
- B-04049047087632
- FDA product code
- GDG
- EMDN code
- L04100299 Digestive system surgical probes, reusable - other
- GMDN term
- Soft-tissue surgical hook, reusable
- Device class
- Class I
- Regulation number
- 878.4800
- EU registration type
- Legacy device (under a directive)
- EU market of registration
- Germany
- GUDID distribution status
- In Commercial Distribution
- Sterilisation method
- Moist Heat or Steam Sterilization
Similar devices in this category
Other devices filed under ABDOMINAL SURGERY INSTRUMENTS, REUSABLE.