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Via 00719702

by US Endoscopy 2 variants

Via 00719702 is a Class II device made by US Endoscopy, listed in FDA GUDID since 17 Sep 2016 (UDI-DI 00816765012918), not in commercial distribution (GUDID) as of 22 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 22 Oct 2026.

Regulatory status

as of registry sync 22 Oct 2026

RegionAuthorizationNumberDateStatus
United StatesGUDID listing Number00816765012918 UDI-DI Date17 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  • Withdrawn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
Via
Generic name
Endoscopy preparation kit
Model / Ref / Catalog
00719702
Primary DI / UDI-DI
00816765012918
FDA product code
NWU
GMDN term
Endoscopy preparation kit
Device class
Class II
Regulation number
876.1500
GUDID distribution status
Not in Commercial Distribution

Similar devices

Other devices filed under FDA product code NWU (Endoscope introducer kit).

Other devices from US Endoscopy

See all devices from US Endoscopy →

Properties

  • Single use
  • Prescription use
  • Convenience kit
  • Premarket exempt
  • Lot / batch number
  • Expiration date
Other properties (9, all answered No)