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Monarch RT 307

by Meridian Medical Systems, LLC

Monarch RT 307 is a Class II device made by Meridian Medical Systems, LLC, listed in FDA GUDID since 24 Sep 2016 (UDI-DI 00851354007104), 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 Number00851354007104 UDI-DI Date24 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  • Withdrawn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
Monarch
Generic name
Flat panel x-ray detector integration unit
Model / reference
RT 307
Primary DI / UDI-DI
00851354007104
FDA product code
MQB
GMDN term
Flat panel x-ray detector integration unit
Device class
Class II
Regulation number
892.1680
GUDID distribution status
In Commercial Distribution

Related devices

Category: Flat panel x-ray detector integration unit

Similar devices

Other devices filed under FDA product code MQB (Solid State X-Ray Imager (Flat Panel/Digital Imager)).

Other devices from Meridian Medical Systems, LLC

See all devices from Meridian Medical Systems, LLC →

Properties

  • Prescription use
  • Serial number
  • Manufacturing date
Other properties (12, all answered No)