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VS3-Ir 153-0052

by Visionsense Ltd.

VS3-Ir 153-0052 is a Class II device made by Visionsense Ltd., listed in FDA GUDID since 23 Sep 2016 (UDI-DI 18130400103427), 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 Number18130400103427 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  • Withdrawn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-Ir
Generic name
Endoscope video camera
Model / Ref / Catalog
153-0052
Primary DI / UDI-DI
18130400103427
FDA product code
HRX, GCJ
GMDN term
Endoscope video camera
Device class
Class II
Regulation number
888.1100, 876.1500
GUDID distribution status
In Commercial Distribution

Related devices

Category: Endoscope video camera

Similar devices in this category

Other devices filed under Endoscope video camera.

Other devices from Visionsense Ltd.

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Properties

  • Sterilise before use
  • Prescription use
  • Serial number
  • Manufacturing date
Other properties (11, all answered No)