6 results
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17ms
·
Sources: EU EUDAMED, US FDA
Filters
Regulation: Us FDA
×
QUINTEST
FDA 510(k)
FDA Class 2
·General Hospital
ECG-ELECTRODE(SWAROMED)
FDA 510(k)
FDA Class 2
·Cardiovascular
DeltaWave Nasal Pillow System
FDA 510(k)
FDA Class 2
·Anesthesiology
X8000 LIGHTSOURCE
FDA Adverse Event
Malfunction
·STRYKER ENDOSCOPY SAN JOSE·Product code FCW·December 16, 2010
HEART START XL
FDA Adverse Event
Malfunction
·PHILIPS MEDICAL SYSTEMS·Product code MKJ·January 14, 2013
REFLEX HYBRID REVISION DRIVER DRAW ROD SCREW EXTRACTOR
FDA Adverse Event
Malfunction
·STRYKER SPINE-FRANCE·Product code LXH·July 23, 2014