BEUDAMED
    8 results · 18ms · Sources: EU EUDAMED, US FDA

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    Q-PAK THERAPEUTIC DRUG MONIT. CONTROL S

    FDA 510(k)
    FDA Class 1 ·Clinical Toxicology

    GUTHRIE SHIELD PLUS BLUE LATEX EXAMINATION GLOVES (POWDER-FREE)

    FDA 510(k)
    FDA Class 1 ·General Hospital

    EXTRICARE

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

    VAPR3 FOOTSWITCH *EA

    FDA Adverse Event
    Malfunction ·DEPUY MITEK LLC US·Product code HRX·February 11, 2021

    MINI-INFUSER RADIATION STERILIZED EXTENSION SETS

    FDA Adverse Event
    Malfunction ·BAXTER HEALTHCARE CORPORATION·Product code FPA·May 7, 2021

    NATURALYTE

    FDA Adverse Event
    Death ·FRESENIUS MEDICAL CARE NORTH AMERICA·Product code KPO·April 25, 2014

    ONETOUCHPING GLUCOSEMGMTSYSTEM

    FDA Adverse Event
    Malfunction ·ANIMAS CORPORATION·Product code LZG·October 31, 2012

    CONSTRAINED ACETABULAR INSERTS

    FDA Adverse Event
    Injury ·STRYKER ORTHOPAEDICS MAHWAH·Product code KWZ·August 16, 2010