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Gimmi QS.1881.00

by Gimmi GmbH

Ref QS.1881.00

Gimmi QS.1881.00 is a Class I device made by Gimmi GmbH, registered in EUDAMED on 8 Sep 2026 (Basic UDI-DI B-04049047081548) and listed in FDA GUDID since 22 May 2025 (UDI-DI 04049047081548), active as of 25 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 25 Oct 2026.

Regulatory status

as of registry sync 25 Oct 2026

RegionAuthorizationNumberDateStatus
European UnionCE/MDD EUDAMED NumberB-04049047081548 Basic UDI-DI 04049047081548UDI-DIDate8 Sep 2026RegisteredStatusActive
United StatesGUDID listing GUDID Number04049047081548 UDI-DI Date22 May 2025ListedStatusListed GUDID: in commercial distribution

Official records

Across registries

2 registries list this device

  • EUDAMED Basic UDI-DI B-04049047081548 registered 8 Sep 2026 Active
  • FDA GUDID UDI-DI 04049047081548 listed 22 May 2025 Listed

Timeline

2 dated events

  1. Listed FDA GUDID 04049047081548
  2. Registered EUDAMED B-04049047081548

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  • Withdrawn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
Bone file/rasp, manual, reusable
Device name
Wiener Antrum Rasp
Model / Ref / Catalog
QS.1881.00
Description
WIENER ANTRUM RASP FIG. 2 LENGTH 180 MM
Primary DI / UDI-DI
04049047081548
Basic UDI-DI
B-04049047081548
FDA product code
KBA
EMDN code
L149099 ENT instruments, reusable - other
GMDN term
Bone file/rasp, manual, reusable
Device class
Class I
Regulation number
874.4420
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: Bone file/rasp, manual, reusable

Similar devices in this category

Other devices filed under ENT INSTRUMENTS, REUSABLE - OTHER.

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Properties

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