MedRx Avant REMsp

MedRx Avant REMsp is a Class II device made by Medrx, Inc., listed in FDA GUDID since 24 Sep 2016 (UDI-DI 00810044580075), 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

Source GUDID, synced 22 Oct 2026.

Regulatory status

as of registry sync 22 Oct 2026

Region	Authorization	Number	Date	Status
United States	GUDID listing	Number00810044580075 UDI-DI	Date24 Sep 2016Listed	StatusListed GUDID: in commercial distribution

Official records

AccessGUDID record UDI-DI 00810044580075

Coverage

1 jurisdiction

Active
Expiring
Withdrawn
Listed
Not covered

United States — GUDID listing Listed

Specification

GUDID

Trade name: MedRx
Generic name: Audiometric/hearing aid tester
Model / reference: Avant REMsp

Primary DI / UDI-DI: 00810044580075
FDA product code: ETW
GMDN term: Audiometric/hearing aid tester

Device class: Class II
Regulation number: 874.3310
GUDID distribution status: In Commercial Distribution

Similar devices in this category

Other devices filed under Audiometric/hearing aid tester.

Other devices from Medrx, Inc.

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Properties

Premarket exempt
Serial number
Manufacturing date

Other properties (12, all answered No)