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Cios Alpha 10308191

by Siemens Healthcare GmbH

Cios Alpha 10308191 is a portable general-purpose fluoroscopic x-ray system (FDA Class II) made by Siemens Healthcare GmbH, listed in FDA GUDID since 24 Sep 2016 (UDI-DI 04056869009032), registry data as of 12 Nov 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 12 Nov 2026.

Regulatory status

as of registry sync 12 Nov 2026

RegionAuthorizationNumberDateStatus
United StatesGUDID listing Number04056869009032 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  • Withdrawn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

Trade name
Cios Alpha
Generic name
Portable general-purpose fluoroscopic x-ray system, digital
Model / reference
10308191
Primary DI / UDI-DI
04056869009032
FDA product code
OXO, OWB
GMDN term
Portable general-purpose fluoroscopic x-ray system, digital
Device class
Class II
Regulation number
892.1650
GUDID distribution status
In Commercial Distribution

Related devices

Category: Portable general-purpose fluoroscopic x-ray system, digital

Similar devices in this category

Other devices filed under Portable general-purpose fluoroscopic x-ray system, digital.

Other devices from Siemens Healthcare GmbH

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Properties

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