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Gimmi E.8000.01

by Gimmi GmbH

Gimmi E.8000.01 is a Class II device made by Gimmi GmbH, listed in FDA GUDID since 5 May 2017 (UDI-DI 04049047041993), registry data as of 23 Oct 2026.

Listed FDA GUDID listing, no authorization on record

Valid until

Not applicable

Database listing, no authorization

FDA recalls

Not checked

No FDA submission to match recalls against

Documents

None

No authorization documents

Trust

Unverified

Source GUDID, synced 23 Oct 2026.

Regulatory status

as of registry sync 23 Oct 2026

RegionAuthorizationNumberDateStatus
United StatesGUDID listing Number04049047041993 UDI-DI Date5 May 2017ListedStatusListed GUDID: in commercial distribution

Official records

Coverage

1 jurisdiction

United States of America
  • Active
  • Expiring
  • Withdrawn
  • Listed
  • Not covered

United States — GUDID listing Listed

Specification

GUDID

Trade name
Gimmi
Generic name
Endoscopic light source adaptor
Model / Ref / Catalog
E.8000.01
Description
ADAPTOR FOR FIBRE OPTIC LIGHT CABLE, GIMMI 3.5/4.8 MM PROJECTOR END
Primary DI / UDI-DI
04049047041993
FDA product code
GCJ
GMDN term
Endoscopic light source adaptor
Device class
Class II
Regulation number
876.1500
GUDID distribution status
In Commercial Distribution
Sterilisation method
Moist Heat or Steam Sterilization

Related devices

Category: Endoscopic light source adaptor

Other devices from Gimmi GmbH

See all devices from Gimmi GmbH →

Properties

  • Sterilise before use
  • Prescription use
  • Lot / batch number
Other properties (12, all answered No)