BEUDAMED
    7 results · 27ms · Sources: EU EUDAMED, US FDA

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    ASTRA T2, T3, T4, T6 PULSE GENERATORS NEW PACKAGE

    FDA 510(k)
    FDA Class 3 ·Cardiovascular

    FlexCare Rescue 8907-85 200*85*13cm

    Device
    EU MDR · Eu Md Class 1 ·Vevia Finland Oy·On the market

    MRI COMPATIBLE PATIENT MONITORING SYSTEM, MODEL 865214

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    Reprocessed PentaRay Nav eco High-Density Mapping Catheter

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    PINNACLE MTL INS NEUT44IDX64OD

    FDA Adverse Event
    Injury ·DEPUY ORTHOPAEDICS, INC. 1818910·Product code KWA·June 24, 2014

    TERUMO CDI 500 BLOOD PARAMETER MONITOR

    FDA Adverse Event
    Malfunction ·TERUMO CARDIOVASCULAR SYSTEMS CORP.·Product code DRY·November 1, 2010

    NEXGEN LCCK ARTICULAR SURFACE

    FDA Adverse Event
    Injury ·ZIMMER, INC.·Product code JWH·December 21, 2012