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S.7048.16

by Gimmi GmbH

Ref S.7048.16

S.7048.16 is a Class I device made by Gimmi GmbH, registered in EUDAMED on 8 Sep 2026 (Basic UDI-DI B-04049047092131) and listed in FDA GUDID since 15 Jun 2023 (UDI-DI 04049047092131), active as of 24 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 24 Oct 2026.

Regulatory status

as of registry sync 24 Oct 2026

RegionAuthorizationNumberDateStatus
European UnionCE/MDD EUDAMED NumberB-04049047092131 Basic UDI-DI 04049047092131UDI-DIDate8 Sep 2026RegisteredStatusActive
United StatesGUDID listing GUDID Number04049047092131 UDI-DI Date15 Jun 2023ListedStatusListed GUDID: in commercial distribution

Official records

Across registries

2 registries list this device

  • EUDAMED Basic UDI-DI B-04049047092131 registered 8 Sep 2026 Active
  • FDA GUDID UDI-DI 04049047092131 listed 15 Jun 2023 Listed

Timeline

2 dated events

  1. Listed FDA GUDID 04049047092131
  2. Registered EUDAMED B-04049047092131

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  • Withdrawn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

Generic name
Rigid endoscopic biopsy forceps, reusable
Model / reference
S.7048.16
Description
GRASPING FORCEPS FLEXIBLE; Ø 1.6 MM / 5 CH, ALLIGATOR JAW; WORKING LENGTH 400 MM
Primary DI / UDI-DI
04049047092131
Basic UDI-DI
B-04049047092131
FDA product code
FCL
EMDN code
L060403 Endoscopic urology forceps, reusable
GMDN term
Rigid endoscopic biopsy forceps, reusable
Device class
Class I
Regulation number
876.1075
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: Rigid endoscopic biopsy forceps, reusable

Similar devices in this category

Other devices filed under ENDOSCOPIC UROLOGY FORCEPS, REUSABLE.

Other devices from Gimmi GmbH

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Properties

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