3 results
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36ms
·
Sources: EU EUDAMED, US FDA
Filters
FDA Adverse Event
×
OT VERIO PRO METER
FDA Adverse Event
Malfunction
·LIFESCAN EUROPE, A DIVISION OF CILAG GMBH INTL·Product code NBW·February 14, 2013
19MM MOD REV HIP BDY/BLT +20MMCOMPONENT LEVEL 9006
FDA Adverse Event
Malfunction
·STRYKER ORTHOPAEDICS CORK·Product code LZO·December 21, 2010
LIBRA XP
FDA Adverse Event
Injury
·ST. JUDE MEDICAL - NEUROMODULATION·Product code LGW·July 23, 2014