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VIA Custom Procedure Kit

by US Endoscopy 3 variants

VIA Custom Procedure Kit (00717442) is a Class II device made by US Endoscopy, listed in FDA GUDID since 6 Mar 2026 (UDI-DI 00724995362645), 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 Number00724995362645 UDI-DI Date6 Mar 2026ListedStatusListed 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  • Withdrawn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
Via
Generic name
Endoscopy preparation kit
Model / Ref / Catalog
VIA Custom Procedure Kit, 00717442
Primary DI / UDI-DI
00724995362645
FDA product code
NWU
GMDN term
Endoscopy preparation kit
Device class
Class II
Regulation number
876.1500
GUDID distribution status
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)