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

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    AESCULAP THORACOSCOPIC INSTRUMENTS

    FDA 510(k)
    FDA Class 2 ·Gastroenterology, Urology

    SERALYZER POTASSIUM REAGENT STRIPS, TEST MODULE, &

    FDA 510(k)
    FDA Class 2 ·Clinical Chemistry

    CONSUMER SENSORY PRODUCTS BIO-LOG 8000

    FDA 510(k)
    FDA Class 2 ·General Hospital

    SYNFRAME RING CLAMP

    FDA Adverse Event
    Injury ·SYNTHES GMBH·Product code LXH·February 1, 2013

    MINICAP

    FDA Adverse Event
    Malfunction ·BAXTER HEALTHCARE - GUANGZHOU·Product code KDI·July 18, 2014

    DEXTRUS

    FDA Adverse Event
    Injury ·EXTERNAL MANUFACTURER·Product code NVN·January 3, 2011

    Allura Exper FD Series. System codes 722003 722010 722022 722005 722011 722019 722001 722002 722006 722012 722008 722013 722020 722025 722015 722023 722038 889006 889016 889009 722005 The device is an X-Ray Generator.

    FDA Enforcement
    Class II ·Terminated·Philips North America, LLC·March 25, 2020