BEUDAMED
    11 results · 19ms · Sources: EU EUDAMED, US FDA

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    CT 8000 DIGITAL INJECTION SYSTEM

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    UniTip Catheter

    FDA UDI
    Unisensor AG·07640172971390·

    FRESENIUS MEDICAL TREATMENT CHAIR T688 SERIES

    FDA 510(k)
    FDA Class 2 ·Physical Medicine

    POWER DRIVE

    FDA 510(k)
    FDA Class 1 ·Dental

    AIA-360

    FDA Adverse Event
    Malfunction ·TOSOH CORPORATION·Product code KHO·March 7, 2020

    SPECTRUM INFUSION PUMP

    FDA Adverse Event
    Malfunction ·BAXTER HEALTHCARE CORP·Product code FRN·January 14, 2014

    MWA PERCUTANEOUS ANTENNA 17CM

    FDA Adverse Event
    Malfunction ·COVIDIEN LP (VALLEYLAB)·Product code NEY·November 18, 2010

    S5 MAST ROLLER PUMP

    FDA Adverse Event
    Other ·SORIN GROUP DEUTSCHLAND·Product code DTQ·December 21, 2012

    WITTICH NITINOL STONE BASKET

    FDA Adverse Event
    Malfunction ·COOK INC·Product code LQR·February 20, 2019

    WITTICH NITINOL STONE BASKET

    FDA Adverse Event
    Malfunction ·COOK INC·Product code LQR·February 20, 2019

    Exactech Equinoxe GLENOID,KEELED, CEMENTED, mates with 47, 50, 53 head, beta curvature, Sizes: a) Small, Item Number 314-01-12, b) Medium, Item Number 314-01-13, c) Large, Item Number 314-01-14, Shoulder Arthroplasty

    FDA Enforcement
    Class II ·Ongoing·Exactech, Inc.·April 10, 2024