Skip to content

GF50A

by Samsung Electronics Co., Ltd.

GF50A is a Class II device made by Samsung Electronics Co., Ltd., listed in FDA GUDID since 24 Sep 2016 (UDI-DI 08806088351889), 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 Number08806088351889 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  • Withdrawn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

Generic name
Stationary basic diagnostic x-ray system, digital
Model / reference
GF50A
Primary DI / UDI-DI
08806088351889
FDA product code
KPR, MQB
GMDN term
Stationary basic diagnostic x-ray system, digital
Device class
Class II
Regulation number
892.1680
GUDID distribution status
In Commercial Distribution

Similar devices in this category

Other devices filed under Stationary basic diagnostic x-ray system, digital.

Other devices from Samsung Electronics Co., Ltd.

See all devices from Samsung Electronics Co., Ltd. →

Properties

  • Prescription use
  • Serial number
Other properties (13, all answered No)