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Gimmi T.0050.23

by Gimmi GmbH

Ref T.0050.23

Gimmi T.0050.23 is a device classified as Class IIb in the EU and Class II in the US made by Gimmi GmbH, registered in EUDAMED on 8 Sep 2026 (Basic UDI-DI B-04049047096610) and listed in FDA GUDID since 5 May 2017 (UDI-DI 04049047096610), 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-04049047096610 Basic UDI-DI 04049047096610UDI-DIDate8 Sep 2026RegisteredStatusActive
United StatesGUDID listing GUDID Number04049047096610 UDI-DI Date5 May 2017ListedStatusListed GUDID: in commercial distribution

Official records

Across registries

2 registries list this device

  • EUDAMED Basic UDI-DI B-04049047096610 registered 8 Sep 2026 Active
  • FDA GUDID UDI-DI 04049047096610 listed 5 May 2017 Listed

Timeline

2 dated events

  1. Listed FDA GUDID 04049047096610
  2. Registered EUDAMED B-04049047096610

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  • Withdrawn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
AlphaActiveGrip EUDAMED
Gimmi GUDID
Generic name
Endoscopic electrosurgical handpiece/electrode, bipolar, reusable
Model / Ref / Catalog
T.0050.23
Primary DI / UDI-DI
04049047096610
Basic UDI-DI
B-04049047096610
FDA product code
HET
EMDN code
L180202 Endoscopic electrosurgery scissors, reusable
GMDN term
Endoscopic electrosurgical handpiece/electrode, bipolar, reusable
Device class
Class IIb EUDAMED
Class II GUDID
Regulation number
884.1720
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

Truth per registry

2 sources · 1 field differs

FieldEUDAMEDGUDID
Device classEUDAMED
Class IIb
GUDID
Class II

Device class is stated on each registry's own scale: Class IIb in the EU (EUDAMED), Class II in the US (FDA GUDID). EU and US classes are different schemes, so this is not a disagreement.

Related devices

Category: Endoscopic electrosurgical handpiece/electrode, bipolar, reusable

Other devices from Gimmi GmbH

See all devices from Gimmi GmbH →

Properties

  • Sterilise before use
  • Reusable
  • Prescription use
  • Lot / batch number
Other properties (21, all answered No)