BEUDAMED
    7 results · 27ms · Sources: EU EUDAMED, US FDA

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    BURTON SLIT LAMP - MODEL 2000

    FDA 510(k)
    FDA Class 2 ·Ophthalmic

    SUCTION/IRRIGATION PROBE

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

    ANSWER QUICK AND SIMPLE AT-HOME PREGNANCY TEST

    FDA 510(k)
    FDA Class 2 ·Clinical Chemistry

    AMK TIB INS SIZE 1 12MM

    FDA Adverse Event
    Injury ·DEPUY-RAYNHAM, A DIV. OF DEPUY ORTHOPAEDICS·Product code JWH·January 22, 2013

    SPECTRUM INFUSION PUMP

    FDA Adverse Event
    Malfunction ·BAXTER HEALTHCARE CORP·Product code FRN·February 5, 2014

    FORCE FX-C GENERATOR

    FDA Adverse Event
    Malfunction ·COVIDIEN LP (VALLEYLAB)·Product code GEI·December 10, 2010

    OPTETRAK Comprehensive Knee System including OPTETRAK RBK PS Tibial Components. NOTE: Information reflects Exactech recall expansion initiated on 02/07/2022.

    FDA Enforcement
    Class II ·Ongoing·Exactech, Inc.·October 13, 2021