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Multiple Loop Polypectomy Snare 92668

by Avanos Medical, Inc.

Multiple Loop Polypectomy Snare 92668 (60413) is a Class II device made by Avanos Medical, Inc., listed in FDA GUDID since 27 Jul 2019 (UDI-DI 00350770926681), 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 Number00350770926681 UDI-DI Date27 Jul 2019ListedStatusListed 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  • Withdrawn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
Multiple Loop Polypectomy Snare
Generic name
Mechanical-cutting endoscopic polypectomy snare
Model / Ref / Catalog
92668, 60413
Primary DI / UDI-DI
00350770926681
FDA product code
FDI
GMDN term
Mechanical-cutting endoscopic polypectomy snare
Device class
Class II
Regulation number
876.4300
GUDID distribution status
In Commercial Distribution

Related devices

Category: Mechanical-cutting endoscopic polypectomy snare

Similar devices in this category

Other devices filed under Mechanical-cutting endoscopic polypectomy snare.

Other devices from Avanos Medical, Inc.

See all devices from Avanos Medical, Inc. →

Properties

  • Supplied sterile
  • Single use
  • Prescription use
  • Lot / batch number
  • Expiration date
  • Manufacturing date
Other properties (9, all answered No)