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Gimmi AC.1130.05

by Gimmi GmbH

Ref AC.1130.05

Gimmi AC.1130.05 is a Class I device made by Gimmi GmbH, registered in EUDAMED on 16 Sep 2026 (Basic UDI-DI B-04049047685524) and listed in FDA GUDID since 23 Apr 2025 (UDI-DI 04049047685524), active as of 23 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 23 Oct 2026.

Regulatory status

as of registry sync 23 Oct 2026

RegionAuthorizationNumberDateStatus
European UnionCE/MDD EUDAMED NumberB-04049047685524 Basic UDI-DI 04049047685524UDI-DIDate16 Sep 2026RegisteredStatusActive
United StatesGUDID listing GUDID Number04049047685524 UDI-DI Date23 Apr 2025ListedStatusListed GUDID: in commercial distribution

Official records

Across registries

2 registries list this device

  • EUDAMED Basic UDI-DI B-04049047685524 registered 16 Sep 2026 Active
  • FDA GUDID UDI-DI 04049047685524 listed 23 Apr 2025 Listed

Timeline

2 dated events

  1. Listed FDA GUDID 04049047685524
  2. Registered EUDAMED B-04049047685524

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  • Withdrawn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
Scalp wound clip
Model / Ref / Catalog
AC.1130.05
Description
SCHWARTZ FORCEPS 25° ANGLED, SMOOTH, CA. 5.0 N 10 X 1.7 MM, NOT FOR NEURO AND CARDIO
Primary DI / UDI-DI
04049047685524
Basic UDI-DI
B-04049047685524
FDA product code
DWS
EMDN code
L07080199 Vascular surgery clamps, reusable - other
GMDN term
Scalp wound clip
Device class
Class I
Regulation number
870.4500
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

Related devices

Category: Scalp wound clip

Similar devices in this category

Other devices filed under CARDIOVASCULAR SURGERY INSTRUMENTS, REUSABLE.

Other devices from Gimmi GmbH

See all devices from Gimmi GmbH →

Properties

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