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Mdr-600HD 1921062050

by Dongguan Teac Electronics Co., Ltd.

Mdr-600HD 1921062050 is a Class I device made by Dongguan Teac Electronics Co., Ltd., listed in FDA GUDID since 24 Sep 2020 (UDI-DI 04573499760015), 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 Number04573499760015 UDI-DI Date24 Sep 2020ListedStatusListed 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  • Withdrawn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
Mdr-600HD
Generic name
Medical video image recorder
Model / reference
1921062050
Primary DI / UDI-DI
04573499760015
FDA product code
LMB
GMDN term
Medical video image recorder
Device class
Class I
Regulation number
892.2010
GUDID distribution status
In Commercial Distribution

Similar devices

Other devices filed under FDA product code LMB (Device, Digital Image Storage, Radiological).

Other devices from Dongguan Teac Electronics Co., Ltd.

See all devices from Dongguan Teac Electronics Co., Ltd. →

Properties

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