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VS3-Ir 145-0041

by Visionsense Ltd.

VS3-Ir 145-0041 is a Class II device made by Visionsense Ltd., listed in FDA GUDID since 1 Apr 2021 (UDI-DI 10884521810167), 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 Number10884521810167 UDI-DI Date1 Apr 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  • Withdrawn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
Endoscopic video image processing/light source system
Model / Ref / Catalog
145-0041
Primary DI / UDI-DI
10884521810167
FDA product code
OWN
GMDN term
Endoscopic video image processing/light source system
Device class
Class II
Regulation number
876.1500
GUDID distribution status
In Commercial Distribution

Related devices

Category: Endoscopic video image processing/light source system

Similar devices in this category

Other devices filed under Endoscopic video image processing/light source system.

Other devices from Visionsense Ltd.

See all devices from Visionsense Ltd. →

Properties

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