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

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    MAVIG ANGIO SHIELD MODELS 6290 & 6272

    FDA 510(k)
    FDA Class 1 ·Radiology

    De Soutter Medical

    FDA UDI
    DE SOUTTER MEDICAL LIMITED·05051471123014·K-WIRE - SINGLE TROCAR 2.0mm DIA x 150mm

    ARS-EKG 12K INTERPRETIVE ELECTROCARDIOGRAPHY SYST

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    EUGONIC AGAR

    FDA 510(k)
    FDA Class 1 ·Microbiology

    RESTORE ULTRA

    FDA Adverse Event
    Malfunction ·MDT PUERTO RICO OPERATIONS CO., JUNCOS·Product code LGW·December 8, 2010

    EXTENSION SET

    FDA Adverse Event
    Injury ·BAXTER HEALTHCARE - MOUNTAIN HOME·Product code KDJ·January 30, 2013

    SPECTRUM INFUSION PUMP

    FDA Adverse Event
    Malfunction ·BAXTER HEALTHCARE CORPORATION·Product code FRN·February 1, 2014

    DeRoyal CHILDREN'S GENERAL TRACEPACK, REF 89-9342-06

    FDA Recall
    Open, Classified ·DeRoyal Industries Inc·Product code LRO·October 3, 2024

    DeRoyal CHILDREN'S GENERAL TRACEPACK, REF 89-9342-06

    FDA Enforcement
    Class II ·Ongoing·DeRoyal Industries Inc·November 13, 2024