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Centurion®, Intrepid® 8065753137

by Alcon Laboratories, Inc.

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 23 Oct 2026. What this means

Regulatory status

as of registry sync 23 Oct 2026

RegionAuthorizationNumberDateStatus
United StatesGUDID listing Number00380657531370 UDI-DI Date22 Nov 2019ListedStatusListed 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  • Withdrawn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
Centurion®, Intrepid®
Generic Name
Ophthalmic surgical procedure kit, non-medicated, single-use
Model / Reference
8065753137
Description
CENTURION® Vision System Active FMS w/ INTREPID Nano Sleeves, 0.9MM 45° ABS* INTERPID Hybrid Tip
Primary DI / UDI-DI
00380657531370
FDA Product Code
HQC
GMDN Term
Ophthalmic surgical procedure kit, non-medicated, single-use
Device Class
Class II
Regulation Number
886.4670
GUDID distribution status
In Commercial Distribution

Related devices

Category: Ophthalmic surgical procedure kit, non-medicated, single-use

Other devices from Alcon Laboratories, Inc.

See all devices from Alcon Laboratories, Inc. →

Properties

  • Sterile
  • Single Use
  • Prescription Use
  • Lot / Batch Number
  • Serial 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
  • Premarket Exempt: No