3 results
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23ms
·
Sources: EU EUDAMED, US FDA
Filters
FDA Adverse Event
×
PINNACLE MTL INS NEUT36IDX52OD
FDA Adverse Event
Injury
·DEPUY INTL., LTD. ¿ REG. # 8010379·Product code KWA·June 13, 2014
GREENLIGHT XPS LASER SYSTEM
FDA Adverse Event
Malfunction
·AMERICAN MEDICAL SYSTEMS·Product code GEX·December 11, 2012
M2A 38MM NON-FLARED ONE PIECE CUP 38MM X 50 O.D.
FDA Adverse Event
Injury
·BIOMET ORTHOPEDICS·Product code KWA·October 15, 2010