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Gimmi AD.1867.23

by Gimmi GmbH

Ref AD.1867.23

Gimmi AD.1867.23 is a Class I device made by Gimmi GmbH, registered in EUDAMED on 17 Sep 2026 (Basic UDI-DI B-04049047688853) and listed in FDA GUDID since 29 Apr 2025 (UDI-DI 04049047688853), 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-04049047688853 Basic UDI-DI 04049047688853UDI-DIDate17 Sep 2026RegisteredStatusActive
United StatesGUDID listing GUDID Number04049047688853 UDI-DI Date29 Apr 2025ListedStatusListed GUDID: in commercial distribution

Official records

Across registries

2 registries list this device

  • EUDAMED Basic UDI-DI B-04049047688853 registered 17 Sep 2026 Active
  • FDA GUDID UDI-DI 04049047688853 listed 29 Apr 2025 Listed

Timeline

2 dated events

  1. Listed FDA GUDID 04049047688853
  2. Registered EUDAMED B-04049047688853

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  • Withdrawn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
Self-retaining surgical retractor, reusable
Device name
Charnley Blade Large
Model / Ref / Catalog
AD.1867.23
Description
CHARNLEY BLADE LARGE ONLY 25 X 75 MM
Primary DI / UDI-DI
04049047688853
Basic UDI-DI
B-04049047688853
FDA product code
FFO
EMDN code
L040901 Abdominal spreaders, reusable
GMDN term
Self-retaining surgical retractor, 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

Related devices

Category: Self-retaining surgical retractor, reusable

Similar devices in this category

Other devices filed under ABDOMINAL 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)