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Flaatz 601

by Drtech Corp.

Flaatz 601 is a Class II device made by Drtech Corp., listed in FDA GUDID since 2 Sep 2016 (UDI-DI 08800018402504), 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 Number08800018402504 UDI-DI Date2 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  • Withdrawn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
Flaatz
Generic name
Diagnostic x-ray digital imaging conversion system
Model / reference
FLAATZ 601
Primary DI / UDI-DI
08800018402504
FDA product code
MQB
GMDN term
Diagnostic x-ray digital imaging conversion system
Device class
Class II
Regulation number
892.1680
GUDID distribution status
In Commercial Distribution

Related devices

Category: Diagnostic x-ray digital imaging conversion system

Similar devices

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

Other devices from Drtech Corp.

See all devices from Drtech Corp. →

Properties

  • Premarket exempt
  • Serial number
Other properties (13, all answered No)