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Avanos 94815

by Avanos Medical, Inc.

Avanos 94815 (0112-14LV) is a Class II device made by Avanos Medical, Inc., listed in FDA GUDID since 15 Mar 2019 (UDI-DI 00350770948157), 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 Number00350770948157 UDI-DI Date15 Mar 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  • Withdrawn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
Avanos
Generic name
Gastrostomy tube
Model / Ref / Catalog
94815, 0112-14LV
Primary DI / UDI-DI
00350770948157
FDA product code
KNT
GMDN term
Gastrostomy tube
Device class
Class II
Regulation number
876.5980
GUDID distribution status
In Commercial Distribution
MRI safety
MR Safe
Size
Catheter Gauge — 14 French

Related devices

Category: Gastrostomy tube

Similar devices in this category

Other devices filed under Gastrostomy tube.

Other devices from Avanos Medical, Inc.

See all devices from Avanos Medical, Inc. →

Properties

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