BEUDAMED
    9 results · 17ms · Sources: EU EUDAMED, US FDA

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    AES, (ANESCO EVACUATION SYSTEM) ACTIVE WASTE ANESTHETIC GAS EVACUATION SYSTEM

    FDA 510(k)
    FDA Class 2 ·Anesthesiology

    TOX/See

    FDA UDI
    BIO-RAD LABORATORIES, INC.·00847817000379·TOX/See Drug Screen Test AMP, BZO, COC, OPI, THC

    STERILE SKIN SCRUB TRAYS

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

    SOLUTION SYSTEM CUP

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    PS TIBIAL INSERTS SZ 2, 13MM

    FDA Adverse Event
    Injury ·EXACTECH, INC.·Product code JWH·April 16, 2024

    ANIMAS INSULIN INFUSION PUMP

    FDA Adverse Event
    Malfunction ·ANIMAS CORP.·Product code LZG·December 21, 2010

    DIMENSION® CLINICAL CHEMISTRY SYSTEM

    FDA Adverse Event
    Malfunction ·SIEMENS HEALTHCARE DIAGNOSTICS INC - GLASGOW·Product code MMI·July 18, 2014

    TRANSTAR STRETCHER

    FDA Adverse Event
    Malfunction ·HILL-ROM, INC.·Product code FPO·December 26, 2012

    Bio-Rad brand ''TOX/See Drug Screen Test''; Catalog numbers: 1945182EX, 1945216, 194-5223

    FDA Recall
    Terminated ·Bio-Rad Laboratories Inc·Product code DIO·June 4, 2004