BEUDAMED
    10 results · 20ms · Sources: EU EUDAMED, US FDA

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    Filters Regulation: Us FDA ×

    PERFIX SPINAL SYSTEM, MODEL SNA4530-9610, SNM4530-9610, SN3020 (TOTAL: 549)

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    Ormco

    FDA UDI
    ORMCO CORPORATION·00889989026863·ARCH P/F EDG.RECT.LO170 X250 PK10

    OLYMPUS SUCTION PUMP, MODEL KV-5

    FDA 510(k)
    FDA Class 2 ·General, Plastic Surgery

    HEARTSTREAM XL DEFIBRILLATOR/MONITOR, MODEL M4735A

    FDA 510(k)
    FDA Class 3 ·Cardiovascular

    EZ-IO POWER DRIVER

    FDA Adverse Event
    Malfunction ·TELEFLEX MEDICAL·Product code FMI·December 14, 2020

    CRE FIXED WIRE BALLOON DILATOR

    FDA Adverse Event
    Injury ·BOSTON SCIENTIFIC COKE LTD·Product code KNQ·August 29, 2007

    SPECTRUM MONITOR

    FDA Adverse Event
    Malfunction ·MINDRAY DS USA, INC.·Product code MHX·April 30, 2013

    GRANUFLO

    FDA Adverse Event
    Injury ·FRESENIUS MEDICAL CARE NORTH AMERICA·Product code KPO·August 20, 2014

    CYPHER SIROLIMUS-ELUTING CORONARY STENT

    FDA Adverse Event
    Injury ·CORDIS LLC (PR)·Product code NIQ·May 17, 2011

    EZ-IO POWER DRIVER

    FDA Adverse Event
    Malfunction ·TELEFLEX MEDICAL·Product code FMI·December 14, 2020