10 results
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21ms
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Sources: EU EUDAMED, US FDA
Filters
Regulation: Us FDA
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CONSENUS HIP SYSTEM -- ACETABULAR REAMER
FDA 510(k)
FDA Class 1
·General, Plastic Surgery
TOX/See
FDA UDI
BIO-RAD LABORATORIES, INC.·00847817000737·TOX/See Drug Screen Test BZO
De Soutter Medical
FDA UDI
DE SOUTTER MEDICAL LIMITED·05051471183797·K-WIRE - SINGLE TROCAR 1.8mm DIA x 150mm
De Soutter Medical
FDA UDI
DE SOUTTER MEDICAL LIMITED·05051471123175·K-WIRE - SINGLE TROCAR THREADED 1.8mm DIA x 150mm
7000 SERIES TOTAL KNEE PATELLAR COMPONENTS
FDA 510(k)
FDA Class 2
·Orthopedic
GERI TOTAL HIP SYSTEM
FDA 510(k)
FDA Class 2
·Orthopedic
BRITEBLADE PRO
FDA Adverse Event
Malfunction
·FLEXICARE MEDICAL LIMITED·Product code CCW·December 22, 2010
ENDURANT II
FDA Adverse Event
Death
·MEDTRONIC IRELAND·Product code MIH·July 18, 2014
CADD -SOLIS AMBULATORY INFUSION PUMP
FDA Adverse Event
Malfunction
·SMITHS MEDICAL MD·Product code MEA·December 26, 2012
INTELLIS
FDA Adverse Event
Malfunction
·MEDTRONIC PUERTO RICO OPERATIONS CO.·Product code LGW·December 10, 2019