Ziehm Vision FD

by Ziehm Imaging GmbH

Ziehm Vision FD is a Class II device made by Ziehm Imaging GmbH, listed in FDA GUDID since 12 Mar 2020 (UDI-DI EZIEZIEHMVISIONFD1651), 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

Source GUDID, synced 12 Nov 2026.

Regulatory status

as of registry sync 12 Nov 2026

Region	Authorization	Number	Date	Status
United States	GUDID listing	NumberEZIEZIEHMVISIONFD1651 UDI-DI	Date12 Mar 2020Listed	StatusListed GUDID: in commercial distribution

Coverage

1 jurisdiction

Active
Expiring
Withdrawn
Listed
Not covered

United States — GUDID listing Listed

Specification

GUDID

Generic name: Mobile general-purpose fluoroscopic x-ray system, digital
Model / reference: Vision FD

Primary DI / UDI-DI: EZIEZIEHMVISIONFD1651
FDA product code: OWB, JAA
GMDN term: Mobile general-purpose fluoroscopic x-ray system, digital

Device class: Class II
Regulation number: 892.1650
GUDID distribution status: In Commercial Distribution

Other devices from Ziehm Imaging GmbH

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Class IIb
Ziehm Vision RFD

Class II
Ziehm Vision RFD 3D

Class II
Ziehm Solo FD

Class II

See all devices from Ziehm Imaging GmbH →

Properties

Serial number
Manufacturing date

Other properties (13, all answered No)