Skip to content

Corpak Percutaneous Endoscopic Gastrostomy Tube 090120038

by Avanos Medical, Inc.

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

Registry data, not yet checked by deviCERTS. Source GUDID, synced 23 Oct 2026. What this means

Regulatory status

as of registry sync 23 Oct 2026

RegionAuthorizationNumberDateStatus
United StatesGUDID listing Number00350770454283 UDI-DI Date7 Aug 2020ListedStatusListed GUDID: in commercial distribution

Coverage

1 jurisdiction

United States of America
  • Active
  • Expiring
  • Withdrawn
  • Listed
  • Not covered

United States — GUDID listing Listed

Specification

GUDID

Trade Name
Corpak Percutaneous Endoscopic Gastrostomy Tube
Generic Name
Gastrostomy tube
Model / Ref / Catalog
090120038
Primary DI / UDI-DI
00350770454283
FDA Product Code
KNT
GMDN Term
Gastrostomy tube
Device Class
Class II
Regulation Number
876.5980
GUDID distribution status
In Commercial Distribution

Related devices

Category: Gastrostomy tube

Other devices from Avanos Medical, Inc.

See all devices from Avanos Medical, Inc. →

Properties

  • Single Use
  • Implantable
  • Prescription Use
  • Convenience Kit
  • Lot / Batch Number

Other properties (9)

  • Sterile: No
  • Contains Latex: No
  • Over-the-Counter: No
  • Combination Product: No
  • HCT/P: No
  • Premarket Exempt: No
  • Serial Number: No
  • Expiration Date: No
  • Manufacturing Date: No