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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 European Union. Also listed in GUDID (US).

CE MDD

Valid until

No date given

EUDAMED holds no validity date

FDA recalls

Not checked

No FDA submission to match recalls against

Documents

None linked in EUDAMED

A group certificate may exist

Trust

Unverified

Source EUDAMED, GUDID, synced 24 Oct 2026.

Regulatory status

as of registry sync 24 Oct 2026

RegionAuthorizationNumberDateStatus
European UnionCE/MDD EUDAMED NumberB-04049047109266 Basic UDI-DI 04049047109266UDI-DIDate9 Sep 2026RegisteredStatusActive
United StatesGUDID listing GUDID Number04049047109266 UDI-DI Date27 May 2025ListedStatusListed GUDID: in commercial distribution

Official records

Across registries

2 registries list this device

  • EUDAMED Basic UDI-DI B-04049047109266 registered 9 Sep 2026 Active
  • FDA GUDID UDI-DI 04049047109266 listed 27 May 2025 Listed

Timeline

2 dated events

  1. Listed FDA GUDID 04049047109266
  2. Registered EUDAMED B-04049047109266

Coverage

2 jurisdictions

United States of AmericaSwedenFinlandLatviaEstoniaDenmarkLithuaniaIrelandNetherlandsGermanyPolandFranceBelgiumLuxembourgCzech RepublicSlovakiaAustriaHungaryRomaniaSloveniaBulgariaPortugalSpainItalyCroatiaGreeceMaltaCyprus
  • Active
  • Expiring
  • Withdrawn
  • Listed
  • Not covered
  • European Union CE/MDD Active
  • United States GUDID listing Listed

Specification

EUDAMED · GUDID

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.

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Properties

  • Sterilise before use
  • Reusable
  • Prescription use
  • Premarket exempt
  • Lot / batch number
  • Manufacturing date
Other properties (19, all answered No)