6 results
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26ms
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Sources: EU EUDAMED, US FDA
Filters
Regulation: Us FDA
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STERI-LUB LUBRICATION GEL
FDA 510(k)
FDA Class 1
·General Hospital
HOOD, OPERATING, SURGICAL
FDA 510(k)
FDA Class 2
·General, Plastic Surgery
CORDIS DUAL-CHAMBER PSA MODEL 296A (PACEMAKER)
FDA 510(k)
FDA Class 2
·Cardiovascular
PULSE GEN MODEL 103
FDA Adverse Event
Injury
·CYBERONICS INC·Product code LYJ·February 6, 2013
SELEX/MAGNUM MOD HD 40MM -6
FDA Adverse Event
Injury
·BIOMET ORTHOPEDICS·Product code KWA·July 18, 2014
TELIGEN
FDA Adverse Event
Malfunction
·GUIDANT CRM CLONMEL IRELAND·Product code LWS·January 3, 2011