6 results
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35ms
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Sources: EU EUDAMED, US FDA
Filters
Regulation: Us FDA
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HI-TOPS ELECTRODES 14-8000
FDA 510(k)
FDA Class 2
·Obstetrics/Gynecology
PROMENADE
FDA 510(k)
FDA Class 2
·Anesthesiology
B-D ARTERIAL BLOOD CONTAINMENT DEVICE
FDA 510(k)
FDA Class 2
·Cardiovascular
FRESENIUS 2008K
FDA Adverse Event
Injury
·FRESENIUS MEDICAL CARE NORTH AMERICA·Product code KDI·June 23, 2014
ONETOUCHPING GLUCOSEMGMTSYSTEM
FDA Adverse Event
Malfunction
·ANIMAS CORPORATION·Product code LZG·January 30, 2013
REPLY
FDA Adverse Event
Injury
·SORIN BIOMEDICA C.R.M., S.R.L.·Product code NVZ·December 8, 2010