8 results
·
19ms
·
Sources: EU EUDAMED, US FDA
Filters
Regulation: Us FDA
×
KARL STORZ MODEL 203020 20 EQUIMAT
FDA 510(k)
FDA Class 2
·Obstetrics/Gynecology
STIMPOD NMS460 Nerve Stimulator
FDA 510(k)
FDA Class 2
·Neurology
BABYBEAT CORDLESS
FDA 510(k)
FDA Class 2
·Obstetrics/Gynecology
MENISCAL FASTENER
FDA Adverse Event
Malfunction
·DEPUY MITEK·Product code MBI·February 14, 2013
OCTRODE LEAD KIT, 60CM LENGTH
FDA Adverse Event
Injury
·ST JUDE MEDICAL - NEUROMODULATION DIVISION·Product code LGW·January 12, 2011
BELT CLIP
FDA Adverse Event
Injury
·MEDTRONIC MINIMED·Product code LZG·July 28, 2014
FT3 - FREE TRIIODOTHYRONINE
FDA Adverse Event
Malfunction
·ROCHE DIAGNOSTICS·Product code CDP·October 10, 2014
FT4, FREE THYROXINE
FDA Adverse Event
Malfunction
·ROCHE DIAGNOSTICS·Product code CEC·September 30, 2016