Gimmi AE.1641.20
by Gimmi GmbH
Ref AE.1641.20
Gimmi AE.1641.20 is a Class I device made by Gimmi GmbH, registered in EUDAMED on 7 Aug 2026 (Basic UDI-DI B-04049047021698) and listed in FDA GUDID since 6 May 2025 (UDI-DI 04049047021698), 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-04049047021698 04049047021698 | Date7 Aug 2026 | StatusActive |
| United States | GUDID listing GUDID | Number04049047021698 | Date6 May 2025 | StatusListed |
Official records
- EUDAMED public site B-04049047021698
- AccessGUDID record 04049047021698
Across registries
- EUDAMED Basic UDI-DI B-04049047021698 registered 7 Aug 2026 Active
- FDA GUDID UDI-DI 04049047021698 listed 6 May 2025 Listed
Timeline
- Listed FDA GUDID 04049047021698
- Registered EUDAMED B-04049047021698
Coverage
- Active
- Expiring
- Withdrawn
- Listed
- Not covered
- European Union
- United States
Specification
- Trade name
- Gimmi
- Generic name
- Suturing needle holder, reusable
- Model / Ref / Catalog
- AE.1641.20
- Description
- CRILE-WOOD NEEDLE HOLDER TC LENGTH 200 MM
- Primary DI / UDI-DI
- 04049047021698
- Basic UDI-DI
- B-04049047021698
- FDA product code
- FHQ
- EMDN code
- L0205 Needle holders, reusable
- GMDN term
- Suturing needle holder, reusable
- Device class
- Class I
- Regulation number
- 876.4730
- 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
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