8 results
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17ms
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Sources: EU EUDAMED, US FDA
Filters
Regulation: Us FDA
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SIGNA HFO/I MAGNETIC RESONANCE SYSTEM
FDA 510(k)
FDA Class 2
·Radiology
MICRONJET 600
FDA 510(k)
FDA Class 2
·General Hospital
MyoWorx TM20
FDA 510(k)
FDA Class 2
·Physical Medicine
OCTRODE
FDA Adverse Event
Injury
·ST. JUDE MEDICAL - NEUROMODULATION·Product code GZB·November 5, 2014
RENEW RECEIVER KIT, 16-CHANNEL
FDA Adverse Event
Injury
·ST. JUDE MEDICAL - NEUROMODULATION·Product code GZB·February 4, 2015
ANIMAS INSULIN INFUSION PUMP
FDA Adverse Event
Malfunction
·ANIMAS CORPORATION·Product code LZG·March 7, 2013
CARPENTIER-EDWARDS PHYSIO ANNULOPLASTY RING WITH DURAFLO TREATMENT
FDA Adverse Event
Injury
·EDWARDS LIFESCIENCES·Product code KRH·February 16, 2011
SPRINT QUATTRO SECURE S
FDA Adverse Event
Injury
·MPRI·Product code LWS·August 8, 2014