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Medit AuraVue MA-AAV

by Medit Corp.

Medit AuraVue MA-AAV, a medical image management system (FDA Class I; FDA product code LMD, System, Digital Image Communications, Radiological) made by Medit Corp., was listed in FDA GUDID on 11 May 2026 (UDI-DI 08800026700890); the registry lists it as not in commercial distribution (GUDID) as of 23 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 23 Oct 2026.

Regulatory status

as of registry sync 23 Oct 2026

RegionAuthorizationNumberDateStatus
United StatesGUDID listing Number08800026700890 UDI-DI Date11 May 2026ListedStatusListed 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  • Withdrawn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
Medit AuraVue
Generic name
Medical image management system
Model / reference
MA-AAV
Primary DI / UDI-DI
08800026700890
FDA product code
LMD
GMDN term
Medical image management system
Device class
Class I
Regulation number
892.2020
GUDID distribution status
Not in Commercial Distribution

Similar devices

Other devices filed under FDA product code LMD (System, Digital Image Communications, Radiological).

Other devices from Medit Corp.

See all devices from Medit Corp. →

Properties

  • Prescription use
  • Premarket exempt
Other properties (13, all answered No)