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

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    MIDDLEBROOK 7H10 AGAR

    FDA 510(k)
    FDA Class 1 ·Microbiology

    GC Initial™

    FDA UDI
    Gc America Inc.·15400556701925·GC Initial™ MC Inside IN-46 Brasil, 50g

    GC Initial™

    FDA UDI
    Gc America Inc.·J0228706461·GC Initial™ MC Inside IN-46 Brasil, 50g

    ADHESE ONE

    FDA 510(k)
    FDA Class 2 ·Dental

    ELECTROSURGICAL PATIENT GROUNDING PAD

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

    TDX/TDXFLX CANNABINOIDS REAGENT

    FDA Adverse Event
    Injury ·ABBOTT HEALTH PRODUCTS, INC.·Product code LDJ·November 8, 2006

    TIBIAL ANKLE CLAMP ASSEMBLY

    FDA Adverse Event
    Malfunction ·STRYKER ORTHOPAEDICS-MAHWAH·Product code MBH·June 12, 2014

    STARCLOSE SE VASCULAR CLOSURE SYSTEM

    FDA Adverse Event
    Injury ·ABBOTT VASCULAR-VASCULAR SOLUTIONS·Product code MGB·October 12, 2010

    PRECISION®

    FDA Adverse Event
    Malfunction ·BOSTON SCIENTIFIC NEUROMODULATION·Product code LGW·December 12, 2012

    SPRYSTEP VECTOR KAFO, Custom made device dynamic ankle-foot orthosis (KAFO) non locking, REF #s: 17VKCUS and 17VKCUSX

    FDA Enforcement
    Class II ·Completed·Townsend Design·January 17, 2024