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Neomed* UK

by Avanos Medical, Inc.

Neomed* UK is a Class II device made by Avanos Medical, Inc., listed in FDA GUDID since 27 Aug 2021 (UDI-DI 00350770003382), 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 Number00350770003382 UDI-DI Date27 Aug 2021ListedStatusListed 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  • Withdrawn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
Neomed*
Generic name
Urethral catheterization support kit, urinary drainage
Model / Ref / Catalog
UK
Primary DI / UDI-DI
00350770003382
FDA product code
FCN
GMDN term
Urethral catheterization support kit, urinary drainage
Device class
Class II
Regulation number
876.5250
GUDID distribution status
In Commercial Distribution

Similar devices

Other devices filed under FDA product code FCN (Urinary drainage collection kit, for indwelling catheter).

Other devices from Avanos Medical, Inc.

See all devices from Avanos Medical, Inc. →

Properties

  • Single use
  • Premarket exempt
  • Lot / batch number
  • Expiration date
Other properties (11, all answered No)