Skip to content

Widex M-CIC 440

by Widex A/S 12 variants

Widex M-CIC 440 (21004099) is a Class II device made by Widex A/S, listed in FDA GUDID since 27 Mar 2021 (UDI-DI 05706069953442), registry data as of 22 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 22 Oct 2026.

Regulatory status

as of registry sync 22 Oct 2026

RegionAuthorizationNumberDateStatus
United StatesGUDID listing Number05706069953442 UDI-DI Date27 Mar 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  • Withdrawn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
Widex
Generic name
Air-conduction hearing aid, in-the-ear
Model / Ref / Catalog
M-CIC 440, 21004099
Primary DI / UDI-DI
05706069953442
FDA product code
OSM
GMDN term
Air-conduction hearing aid, in-the-ear
Device class
Class II
Regulation number
874.3305
GUDID distribution status
In Commercial Distribution

Related devices

Category: Air-conduction hearing aid, in-the-ear

Other devices from Widex A/S

See all devices from Widex A/S →

Properties

  • Premarket exempt
  • Serial number
Other properties (13, all answered No)