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Phoenix 1 PHX1

by CONTROL-X Medical Kereskedelmi és Szolgáltató Zártkörűen Működő Részvénytársaság

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

Registry data, not yet checked by deviCERTS. Source GUDID, synced 22 Oct 2026. What this means

Regulatory status

as of registry sync 22 Oct 2026

RegionAuthorizationNumberDateStatus
United StatesGUDID listing Number05999116100023 UDI-DI Date30 Oct 2024ListedStatusListed GUDID: not in commercial distribution

Coverage

1 jurisdiction

United States of America
  • Active
  • Expiring
  • Withdrawn
  • Listed
  • Not covered

United States — GUDID listing Listed

Specification

GUDID

Trade Name
Phoenix 1
Generic Name
Basic diagnostic x-ray system table, powered
Model / Ref / Catalog
PHX1, 2510
Primary DI / UDI-DI
05999116100023
FDA Product Code
IZZ
GMDN Term
Basic diagnostic x-ray system table, powered
Device Class
Class II
Regulation Number
892.1980
GUDID distribution status
Not in Commercial Distribution

Other devices from CONTROL-X Medical Kereskedelmi és Szolgáltató Zártkörűen Működő Részvénytársaság

Properties

  • Premarket Exempt
  • Serial Number
  • Manufacturing Date

Other properties (11)

  • Sterile: No
  • Single Use: No
  • Implantable: No
  • Contains Latex: No
  • Prescription Use: No
  • Over-the-Counter: No
  • Convenience Kit: No
  • Combination Product: No
  • HCT/P: No
  • Lot / Batch Number: No
  • Expiration Date: No