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

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    QUIKSTRIP DIPSCAN X MULTIDRUG SCREENING DEVICE

    FDA 510(k)
    FDA Class 2 ·Clinical Toxicology

    Bioseal Inc.

    FDA UDI
    BIOSEAL·00630094299037·Vaginal Speculum Large

    JETSTREAM G2 SYSTEM, MODELS PV20300 (JETSTREAM G2 CATHETER AND CONTROL POD); PVCN100 (PV CONSOLE)

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    REPRODENT

    FDA 510(k)
    FDA Class 2 ·Dental

    COULTER® ACT DIFF 2 ANALYZER

    FDA Adverse Event
    Malfunction ·BECKMAN COULTER INC·Product code GKZ·December 7, 2010

    CORDLESS DRIVER 3

    FDA Adverse Event
    Malfunction ·STRYKER INSTRUMENTS-KALAMAZOO·Product code HRX·March 5, 2013

    CAPSURE Z NOVUS

    FDA Adverse Event
    Malfunction ·MEDTRONIC PUERTO RICO, INC.·Product code DTB·February 15, 2011

    530G INSULIN PUMP

    FDA Adverse Event
    Malfunction ·MEDTRONIC PUERTO RICO OPERATIONS CO.·Product code OZO·August 7, 2014