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Forceps for removal 23 gauge/0.6 mm cannula with closure valve. 1276.2

by D.O.R.C. Dutch Ophthalmic Research Center (International) B.V.

Listed FDA GUDID listing, not in commercial distribution

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

Registry data, not yet checked by deviCERTS. Source GUDID, synced 23 Oct 2026. What this means

Regulatory status

as of registry sync 23 Oct 2026

RegionAuthorizationNumberDateStatus
United StatesGUDID listing Number08717872003092 UDI-DI Date1 Feb 2021ListedStatusListed GUDID: not 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  • Withdrawn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
Forceps for removal 23 gauge/0.6 mm cannula with closure valve.
Generic Name
Ophthalmic soft-tissue manipulation forceps, tweezers-like, reusable
Model / Ref / Catalog
1276.2
Primary DI / UDI-DI
08717872003092
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
Not in Commercial Distribution
Sterilization Method
Moist Heat or Steam Sterilization

Related devices

Category: Ophthalmic soft-tissue manipulation forceps, tweezers-like, reusable

Other devices from D.O.R.C. Dutch Ophthalmic Research Center (International) B.V.

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Properties

  • Prescription Use
  • Premarket Exempt
  • Manufacturing Date

Other properties (11)

  • Sterile: No
  • Single Use: No
  • Implantable: No
  • Contains Latex: No
  • Over-the-Counter: No
  • Convenience Kit: No
  • Combination Product: No
  • HCT/P: No
  • Lot / Batch Number: No
  • Serial Number: No
  • Expiration Date: No