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

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    CDH HIP SYSTEM

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    De Soutter Medical

    FDA UDI
    DE SOUTTER MEDICAL LIMITED·05051471123298·K-WIRE - DOUBLE TROCAR 2.0mm DIA x 200mm

    Instrument Case

    FDA UDI
    KATENA PRODUCTS, INC.·00841668111024·INSTRUMENT CADDY MEDIUM

    Color Cuff

    FDA UDI
    STRYKER CORPORATION·07613154599776·Non-Sterile Reusable Tourniquet Cuff Single Bla...

    Color Cuff

    FDA UDI
    STRYKER CORPORATION·07613154599790·Non-Sterile Reusable Tourniquet Cuff Single Bla...

    CARDIMA ABLATION SYSTEM

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

    INCITE ANCHORED CERVICAL INTERBODY (ACI) FUSION DEVICE

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    UNKNOWN CERECYTE MICROCOIL

    FDA Adverse Event
    Injury ·MEDOS INTERNATIONAL SARL·Product code KRD·June 14, 2017

    NITE GUARD

    FDA Adverse Event
    Malfunction ·RANIR LLC·Product code OBR·June 2, 2014

    HUT EXT DR FINAL ASSY-REVERSE

    FDA Adverse Event
    Malfunction ·LIEBEL-FLARSHEIM CO.·Product code IXR·January 15, 2013

    SPRINT QUATTRO SECURE

    FDA Adverse Event
    Injury ·MEDTRONIC PUERTO RICO, INC.·Product code LWS·December 13, 2010

    SYNCHROMED II

    FDA Adverse Event
    Injury ·MEDTRONIC NEUROMODULATION·Product code LKK·September 26, 2008