Ziehm Vision FD

GUDID EZIEZIEHMVISIONFD165

Ziehm Imaging GmbH

Mobile general-purpose fluoroscopic x-ray system, digital
Primary Device IDEZIEZIEHMVISIONFD165
NIH Device Record Key48f986ce-0866-4ac4-8e7e-d9c9737c9a29
Commercial Distribution StatusIn Commercial Distribution
Brand NameZiehm Vision FD
Version Model Number302891; 302929
Company DUNS322720541
Company NameZiehm Imaging GmbH
Device Count1
DM Exemptfalse
Pre-market Exemptfalse
MRI Safety StatusLabeling does not contain MRI Safety Information
Human Cell/Tissue Productfalse
Device Kitfalse
Device Combination Productfalse
Single Usefalse
Lot Batchfalse
Serial Numbertrue
Manufacturing Datetrue
Expiration Datefalse
Donation Id Numberfalse
Contains Natural Rubber Latexfalse
Labeled No Natural Rubber Latexfalse
RX Perscriptionfalse
OTC Over-The-Counterfalse

Device Identifiers

Device Issuing AgencyDevice ID
HIBCCEZIEZIEHMVISIONFD165 [Primary]

FDA Pre-market Approvals/Notifications & deNovo

FDA Product Code

OWBInterventional Fluoroscopic X-Ray System

Sterilization

Steralize Prior To Usefalse
Device Is Sterilefalse

Device Entry Metadata

Public Version StatusNew
Device Record StatusPublished
Public Version Number1
Public Version Date2020-03-20
Device Publish Date2020-03-12

On-Brand Devices [Ziehm Vision FD]

EZIEZIEHMVISIONFD165302891; 302929
EZIEZIEHMVISIONFD1651Mobile C-arm

© 2024 FDA.report
This site is not affiliated with or endorsed by the FDA.