7 results
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19ms
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Sources: EU EUDAMED, US FDA
Filters
Regulation: Us FDA
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MANUAL SURGICAL INSRUMENT
FDA 510(k)
FDA Class 2
·General, Plastic Surgery
De Soutter Medical
FDA UDI
DE SOUTTER MEDICAL LIMITED·05051471122765·K-WIRE - SINGLE TROCAR THREADED 1.8mm DIA x 230mm
SLIMMANAGER, MODEL SM-X, SM-E
FDA 510(k)
FDA Class 2
·Cardiovascular
BD MAX CT/GC/TV, BD MAX INSTRUMENT
FDA 510(k)
FDA Class 2
·Immunology
PULSE-GENERATOR, DUAL CHAMBER, IMPLANTABLE
FDA Adverse Event
Malfunction
·MEDTRONIC MILACA, INC.·Product code LWP·February 9, 2013
FLEXTEND
FDA Adverse Event
Injury
·CPI - DEL CARIBE·Product code NVN·January 6, 2011
OT PING METER
FDA Adverse Event
Malfunction
·LIFESCAN EUROPE, A DIVISION OF CILAG GMBH INTL·Product code NBW·July 23, 2014