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VS3 114-0001

by Visionsense Ltd.

VS3 114-0001 is a Class I device made by Visionsense Ltd., listed in FDA GUDID since 23 Sep 2016 (UDI-DI 18130400103229), 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 Number18130400103229 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  • Withdrawn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 sheath, reusable
Model / Ref / Catalog
114-0001
Primary DI / UDI-DI
18130400103229
FDA product code
KAM
GMDN term
Endoscope sheath, reusable
Device class
Class I
Regulation number
878.4800
GUDID distribution status
Not in Commercial Distribution

Other devices from Visionsense Ltd.

See all devices from Visionsense Ltd. →

Properties

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