Skip to content

VS3-Ir 174-0051

by Visionsense Ltd. 2 variants

VS3-Ir 174-0051 is a Class II device made by Visionsense Ltd., listed in FDA GUDID since 10 Aug 2021 (UDI-DI 10813040013988), 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 Number10813040013988 UDI-DI Date10 Aug 2021ListedStatusListed 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  • Withdrawn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
174-0051
Primary DI / UDI-DI
10813040013988
FDA product code
OWN
GMDN term
Endoscope video camera
Device class
Class II
Regulation number
876.1500
GUDID distribution status
In Commercial Distribution
Sterilisation method
Hydrogen Peroxide

Related devices

Category: Endoscope video camera

Similar devices in this category

Other devices filed under Endoscope video camera.

Other devices from Visionsense Ltd.

See all devices from Visionsense Ltd. →

Properties

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