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Roentgen Works 7.0.2

by Brit Systems

Roentgen Works 7.0.2 is a Class I device made by Brit Systems, listed in FDA GUDID since 1 Jan 2026 (UDI-DI 00850631008810), 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 Number00850631008810 UDI-DI Date1 Jan 2026ListedStatusListed 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  • Withdrawn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
Roentgen Works
Generic name
Radiological PACS-dedicated management software
Model / reference
7.0.2
Primary DI / UDI-DI
00850631008810
FDA product code
LMB, LLZ
GMDN term
Radiological PACS-dedicated management software
Device class
Class I
Regulation number
892.2010, 892.2050
GUDID distribution status
In Commercial Distribution

Similar devices

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

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Properties

Other properties (15, all answered No)