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MDR Video Touch 2

by Hyland LLC

MDR Video Touch 2 is a Class II device made by Hyland LLC, listed in FDA GUDID since 26 Sep 2016 (UDI-DI 00850677007082), 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 Number00850677007082 UDI-DI Date26 Sep 2016ListedStatusListed 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  • Withdrawn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 Video Touch
Generic name
Medical video image recorder
Model / reference
2
Primary DI / UDI-DI
00850677007082
FDA product code
LMA
GMDN term
Medical video image recorder
Device class
Class II
Regulation number
892.2030
GUDID distribution status
In Commercial Distribution

Similar devices

Other devices filed under FDA product code LMA (Digitizer, Image, Radiological).

Other devices from Hyland LLC

See all devices from Hyland LLC →

Properties

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