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MedRx Tinnometer

by Medrx, Inc.

MedRx Tinnometer is a Class II device made by Medrx, Inc., listed in FDA GUDID since 28 Aug 2017 (UDI-DI 00810044580082), not in commercial distribution (GUDID) as of 22 Oct 2026.

Listed FDA GUDID listing, not in commercial distribution

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 Number00810044580082 UDI-DI Date28 Aug 2017ListedStatusListed GUDID: not 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  • Withdrawn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
MedRx
Generic name
Tone audiometer
Model / reference
MedRx Tinnometer
Primary DI / UDI-DI
00810044580082
FDA product code
EWO
GMDN term
Tone audiometer
Device class
Class II
Regulation number
874.1050
GUDID distribution status
Not in Commercial Distribution

Similar devices

Other devices filed under FDA product code EWO (Audiometer).

Other devices from Medrx, Inc.

See all devices from Medrx, Inc. →

Properties

  • Premarket exempt
  • Serial number
  • Manufacturing date
Other properties (12, all answered No)