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APELEM PLATINUM dRF

by Apelem

APELEM PLATINUM dRF is a Class II device made by Apelem, listed in FDA GUDID since 23 May 2016 (UDI-DI 03760172650003), not in commercial distribution (GUDID) as of 23 Oct 2026.

Listed FDA GUDID listing, not in commercial distribution

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 Number03760172650003 UDI-DI Date23 May 2016ListedStatusListed GUDID: not 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  • Withdrawn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
Apelem
Generic name
Basic diagnostic x-ray system table, powered
Model / reference
PLATINUM dRF
Primary DI / UDI-DI
03760172650003
FDA product code
JAA
GMDN term
Basic diagnostic x-ray system table, powered
Device class
Class II
Regulation number
892.1650
GUDID distribution status
Not in Commercial Distribution

Related devices

Category: Basic diagnostic x-ray system table, powered

Other devices from Apelem

See all devices from Apelem →

Properties

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