Gimmi UC.1106.22
by Gimmi GmbH
Ref UC.1106.22
Gimmi UC.1106.22 is an open-surgery stone-retrieval forceps (EU MDD Class I; FDA Class I; FDA product code GDJ, Clamp, Surgical, General & Plastic Surgery) made by Gimmi GmbH, registered in EUDAMED on 9 Sep 2026 (Basic UDI-DI B-04049047109266) and listed in FDA GUDID since 27 May 2025 (UDI-DI 04049047109266), active as of 24 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-04049047109266 04049047109266 | Date9 Sep 2026 | StatusActive |
| United States | GUDID listing GUDID | Number04049047109266 | Date27 May 2025 | StatusListed |
Official records
- EUDAMED public site B-04049047109266
- AccessGUDID record 04049047109266
Across registries
- EUDAMED Basic UDI-DI B-04049047109266 registered 9 Sep 2026 Active
- FDA GUDID UDI-DI 04049047109266 listed 27 May 2025 Listed
Timeline
- Listed FDA GUDID 04049047109266
- Registered EUDAMED B-04049047109266
Coverage
- Active
- Expiring
- Withdrawn
- Listed
- Not covered
- European Union
- United States
Specification
- Trade name
- Gimmi
- Generic name
- Open-surgery stone-retrieval forceps
- Model / Ref / Catalog
- UC.1106.22
- Description
- RANDALL KIDNEY STONE FORCEPS FIG. 2 LENGTH 220 MM
- Primary DI / UDI-DI
- 04049047109266
- Basic UDI-DI
- B-04049047109266
- FDA product code
- GDJ
- EMDN code
- L06060101 Kidney stones non-endoscopic forceps, reusable
- GMDN term
- Open-surgery stone-retrieval forceps
- 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 NON-ENDOSCOPIC UROLOGY FORCEPS, REUSABLE.