7 results
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18ms
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Sources: EU EUDAMED, US FDA
Filters
Regulation: Us FDA
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TITANIUM CLASSIC COMPRESSION HIP SCREW SYSTEM
FDA 510(k)
FDA Class 2
·Orthopedic
INFX-8000C, V6.20
FDA 510(k)
FDA Class 2
·Radiology
HEPARIN/PLATELET FACTOR 4 ANTIBODY SERUM PANEL
FDA 510(k)
FDA Class 2
·Hematology
DRUG-ELUTING PERMANENT DEFIBRILLATOR ELECTRODES
FDA Adverse Event
Injury
·MPRI·Product code NVY·February 9, 2013
TRANSTAR STRETCHER
FDA Adverse Event
Malfunction
·HILL-ROM INC.·Product code FPO·January 4, 2011
INFUSOMAT SPACE
FDA Adverse Event
Malfunction
·B. BRAUN MELSUNGEN AG·Product code FRN·July 17, 2014
ev3 Pipeline Flex Embolization Device with Shield Technology. Sold OUS. For neurological endovascular use.
FDA Enforcement
Class I
·Terminated·Micro Therapeutics Inc, Dba Ev3 Neurovascular·April 1, 2020