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VS3 153-0032

by Visionsense Ltd.

VS3 153-0032 is a Class II device made by Visionsense Ltd., listed in FDA GUDID since 23 Sep 2016 (UDI-DI 18130400103168), not in commercial distribution (GUDID) as of 23 Oct 2026.

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

Source GUDID, synced 23 Oct 2026.

Regulatory status

as of registry sync 23 Oct 2026

RegionAuthorizationNumberDateStatus
United StatesGUDID listing Number18130400103168 UDI-DI Date23 Sep 2016ListedStatusListed GUDID: not 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  • Withdrawn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
Endoscope video camera
Model / Ref / Catalog
153-0032
Primary DI / UDI-DI
18130400103168
FDA product code
GWG, OWN, GCJ, HRX
GMDN term
Endoscope video camera
Device class
Class II
Regulation number
882.1480, 876.1500, 888.1100
GUDID distribution status
Not in Commercial Distribution

Other devices from Visionsense Ltd.

See all devices from Visionsense Ltd. →

Properties

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