BEUDAMED
    11 results · 28ms · Sources: EU EUDAMED, US FDA

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    CDC HUMAN INFLUENZA VIRUS REAL-TIME RT-PCR DIAGNOSTIC PANEL, INFLUENZA A/B TYPING KIT

    FDA 510(k)
    FDA Class 2 ·Microbiology

    ORIGEN REINFORCED DUAL LUMEN CATHETER

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    CONTREET FOAM CAVITY DRESSING WITH SILVER, MODEL 9628 (2X4 IN.)

    FDA 510(k)
    FDA Unclassified ·Unknown

    ONETOUCHPING GLUCOSEMGMTSYSTEM

    FDA Adverse Event
    ANIMAS CORPORATION·Product code LZG·October 1, 2014

    AEQUALIS

    FDA Adverse Event
    Injury ·TORNIER SAS·Product code KWS·May 23, 2013

    STRETCHER CHAIR

    FDA Adverse Event
    Malfunction ·STRYKER MEDICAL·Product code FPO·May 12, 2011

    UNKNOWN

    FDA Adverse Event
    Injury ·EL.EN. ELECTRONIC ENGINEERING S.P.A.·Product code GEX·February 20, 2025

    UNKNOWN HIP FEMORAL HEAD

    FDA Adverse Event
    Injury ·DEPUY ORTHOPAEDICS INC US·Product code KWY·October 21, 2019

    UNKNOWN HIP FEMORAL STEM

    FDA Adverse Event
    Injury ·DEPUY ORTHOPAEDICS INC US·Product code KWA·October 21, 2019

    UNKNOWN HIP FEMORAL STEM

    FDA Adverse Event
    Injury ·DEPUY ORTHOPAEDICS INC US·Product code JDI·October 21, 2019

    UNKNOWN BONE CEMENT

    FDA Adverse Event
    Injury ·DEPUY ORTHOPAEDICS INC US·Product code LOD·October 21, 2019