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00713100

by US Endoscopy

00713100 is a Class II device made by US Endoscopy, listed in FDA GUDID since 10 Sep 2020 (UDI-DI 00724995195045), 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 Number00724995195045 UDI-DI Date10 Sep 2020ListedStatusListed 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  • Withdrawn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

Generic name
Inert gas-enhanced electrosurgical system
Model / Ref / Catalog
00713100
Primary DI / UDI-DI
00724995195045
FDA product code
NWI
GMDN term
Inert gas-enhanced electrosurgical system
Device class
Class II
Regulation number
876.4300
GUDID distribution status
In Commercial Distribution

Related devices

Category: Inert gas-enhanced electrosurgical system

Similar devices

Also classified as Inert gas-enhanced electrosurgical system.

Other devices from US Endoscopy

See all devices from US Endoscopy →

Properties

  • Prescription use
  • Convenience kit
  • Premarket exempt
  • Serial number
  • Manufacturing date
Other properties (10, all answered No)