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Gimmi T.8047.12

by Gimmi GmbH

Ref T.8047.12

Gimmi T.8047.12 is a device classified as Class I in the EU and Class II in the US made by Gimmi GmbH, registered in EUDAMED on 14 Sep 2026 (Basic UDI-DI B-04049047639152) and listed in FDA GUDID since 5 May 2017 (UDI-DI 04049047639152), 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-04049047639152 Basic UDI-DI 04049047639152UDI-DIDate14 Sep 2026RegisteredStatusActive
United StatesGUDID listing GUDID Number04049047639152 UDI-DI Date5 May 2017ListedStatusListed GUDID: in commercial distribution

Official records

Across registries

2 registries list this device

  • EUDAMED Basic UDI-DI B-04049047639152 registered 14 Sep 2026 Active
  • FDA GUDID UDI-DI 04049047639152 listed 5 May 2017 Listed

Timeline

2 dated events

  1. Listed FDA GUDID 04049047639152
  2. Registered EUDAMED B-04049047639152

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  • Withdrawn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
Alphaport EUDAMED
Gimmi GUDID
Generic name
Laparoscopic trocar blade, reusable
Model / Ref / Catalog
T.8047.12
Primary DI / UDI-DI
04049047639152
Basic UDI-DI
B-04049047639152
FDA product code
GCJ
EMDN code
L031202 Abdominal trocar, reusable
GMDN term
Laparoscopic trocar blade, reusable
Device class
Class I EUDAMED
Class II GUDID
Regulation number
876.1500
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 I
GUDID
Class II

Device class is stated on each registry's own scale: Class I 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: Laparoscopic trocar blade, reusable

Similar devices in this category

Other devices filed under GENERAL SURGERY INSTRUMENTS, 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)