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Alcon Grieshaber Visco Canalostomy 149.40

by Alcon Laboratories, Inc.

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 Number07612717000469 UDI-DI Date19 Aug 2020ListedStatusListed 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  • Withdrawn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
Alcon Grieshaber Visco Canalostomy
Generic Name
Exploratory blunt needle, single-use
Model / Reference
149.40
Primary DI / UDI-DI
07612717000469
FDA Product Code
HMX
GMDN Term
Exploratory blunt needle, single-use
Device Class
Class I
Regulation Number
886.4350
GUDID distribution status
Not in Commercial Distribution

Other devices from Alcon Laboratories, Inc.

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Properties

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

Other properties (7)

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