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Roth Net 00711052

by US Endoscopy

Roth Net 00711052 is a Class II device made by US Endoscopy, listed in FDA GUDID since 17 Sep 2016 (UDI-DI 00816765010877), 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 Number00816765010877 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  • Withdrawn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
Roth Net
Generic name
Gastrointestinal/airway foreign body retrieval basket, single-use
Model / Ref / Catalog
00711052
Primary DI / UDI-DI
00816765010877
FDA product code
FDI, GCJ
GMDN term
Gastrointestinal/airway foreign body retrieval basket, single-use
Device class
Class II
Regulation number
876.4300, 876.1500
GUDID distribution status
Not in Commercial Distribution
Size
Length — 230 Centimeter
Outer Diameter — 2.5 Millimeter
Width — 3 Centimeter

Similar devices

Other devices filed under FDA product code FDI (SNARE, FLEXIBLE).

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Properties

  • Single use
  • Prescription use
  • Lot / batch number
  • Expiration date
  • Manufacturing date
Other properties (10, all answered No)