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Geiz 2.00.67.G

by Bear-Ent, LLC

Geiz 2.00.67.G is a Class I device made by Bear-Ent, LLC, listed in FDA GUDID since 26 May 2026 (UDI-DI G04320067G0), 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 NumberG04320067G0 UDI-DI Date26 May 2026ListedStatusListed GUDID: in commercial distribution

Coverage

1 jurisdiction

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  • Withdrawn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

United States — GUDID listing Listed

Specification

GUDID

Trade name
Geiz
Generic name
Ophthalmic soft-tissue manipulation forceps, tweezers-like, reusable
Model / Ref / Catalog
2.00.67.G
Description
Jeweler's Forceps, No.7 *** Geiz Line ***
Primary DI / UDI-DI
G04320067G0
FDA product code
HNR
GMDN term
Ophthalmic soft-tissue manipulation forceps, tweezers-like, reusable
Device class
Class I
Regulation number
886.4350
GUDID distribution status
In Commercial Distribution
Sterilisation method
Moist Heat or Steam Sterilization

Other devices from Bear-Ent, LLC

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Properties

  • Sterilise before use
  • Prescription use
  • Premarket exempt
  • Lot / batch number
Other properties (11, all answered No)