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

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    FLUORESCENCE DETECTOR MODEL 420

    FDA 510(k)
    FDA Class 1 ·Clinical Chemistry

    Washbon

    FDA UDI
    ORMCO CORPORATION·00889989043921·UPPER LEFT FIRST MOLAR WASHBON BAND SIZE 31

    equilibrium®

    FDA UDI
    DENTAURUM GmbH & Co.KG·J011780031000·equilibrium® ti -7°Torque, 0°Angulation,22

    HISTOCHEMICAL PAS REACTION SET

    FDA 510(k)
    FDA Class 1 ·Hematology

    Endopath Electrosurgery Probe Plus II

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

    PARIETEX

    FDA Adverse Event
    Injury ·SOFRADIM PRODUCTION SAS·Product code FTL·October 10, 2017

    ENERGEN

    FDA Adverse Event
    Injury ·GUIDANT CRM CLONMEL IRELAND·Product code LWS·October 10, 2012

    SPECTRUM INFUSION PUMP

    FDA Adverse Event
    Malfunction ·BAXTER HEALTHCARE CORPORATION·Product code FRN·December 3, 2013

    OT VERIO2 METER

    FDA Adverse Event
    Malfunction ·LIFESCAN EUROPE, A DIVISION OF CILAG GMBH INTL·Product code NBW·May 19, 2015

    ZILVER PTX DRUG-ELUTING PERIPHERAL STENT

    FDA Adverse Event
    Injury ·COOK IRELAND LTD·Product code NIU·September 24, 2015

    ZILVER PTX DRUG-ELUTING PERIPHERAL STENT

    FDA Adverse Event
    Injury ·COOK IRELAND LTD·Product code NIU·March 6, 2014

    ZILVER PTX DRUG-ELUTING PERIPHERAL STENT

    FDA Adverse Event
    Injury ·COOK IRELAND LTD·Product code NIU·September 14, 2016

    ZILVER PTX DRUG-ELUTING PERIPHERAL STENT

    FDA Adverse Event
    Injury ·COOK IRELAND LTD·Product code NIU·September 13, 2016

    ZILVER PTX DRUG-ELUTING PERIPHERAL STENT

    FDA Adverse Event
    Injury ·COOK IRELAND LTD·Product code NIU·September 13, 2016

    ZILVER PTX DRUG-ELUTING PERIPHERAL STENT

    FDA Adverse Event
    Injury ·COOK IRELAND LTD·Product code NIU·December 21, 2015