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VS3 560-6462

by Visionsense Ltd.

VS3 560-6462 is a Class II device made by Visionsense Ltd., listed in FDA GUDID since 23 Sep 2016 (UDI-DI 18130400103342), 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 Number18130400103342 UDI-DI Date23 Sep 2016ListedStatusListed GUDID: in commercial distribution

Official records

Coverage

1 jurisdiction

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  • Withdrawn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

United States — GUDID listing Listed

Specification

GUDID

Trade name
VS3
Generic name
Fibreoptic light cable, reusable
Model / Ref / Catalog
560-6462
Primary DI / UDI-DI
18130400103342
FDA product code
FST, OWN
GMDN term
Fibreoptic light cable, reusable
Device class
Class II
Regulation number
878.4580, 876.1500
GUDID distribution status
In Commercial Distribution

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Properties

  • Sterilise before use
  • Serial number
  • Manufacturing date
Other properties (12, all answered No)