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Cataract Inst Set - Spokane Anderson 67-0028

by Blink Medical Limited

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

Registry data, not yet checked by deviCERTS. Source GUDID, synced 22 Oct 2026. What this means

Regulatory status

as of registry sync 22 Oct 2026

RegionAuthorizationNumberDateStatus
United StatesGUDID listing Number05056785303015 UDI-DI Date12 Nov 2025ListedStatusListed 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  • Withdrawn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
Cataract Inst Set - Spokane Anderson
Generic Name
Ophthalmic surgical procedure kit, non-medicated, single-use
Model / Reference
67-0028
Primary DI / UDI-DI
05056785303015
FDA Product Code
PZG
GMDN Term
Ophthalmic surgical procedure kit, non-medicated, single-use
Device Class
Class I
Regulation Number
886.4350
GUDID distribution status
In Commercial Distribution

Other devices from Blink Medical Limited

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Properties

  • Sterile
  • Single Use
  • Premarket Exempt
  • Lot / Batch Number
  • Expiration Date

Other properties (9)

  • Implantable: No
  • Contains Latex: No
  • Prescription Use: No
  • Over-the-Counter: No
  • Convenience Kit: No
  • Combination Product: No
  • HCT/P: No
  • Serial Number: No
  • Manufacturing Date: No