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

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    ANGIOGRAPHIC GUIDEWIRE

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    THRUWAY GUIDE WIRES

    FDA Adverse Event
    Injury ·BOSTON SCIENTIFIC - MAPLE GROVE·Product code DQX·March 7, 2011

    ACCU-CHEK Guide Blood Glucose Monitoring System

    FDA 510(k)
    FDA Class 2 ·Clinical Chemistry

    NUTRISAFE 2

    FDA 510(k)
    FDA Class 2 ·Gastroenterology, Urology

    ULTRATHANE COOK - COPE TYPE LOCKING LOOP MULTIPURPOSE DRAINAGE CATHETER

    FDA Adverse Event
    Injury ·COOK INC·Product code GBO·April 9, 2014

    PINNACLE MTL INS NEUT40IDX58OD

    FDA Adverse Event
    Injury ·DEPUY ORTHOPAEDICS, INC. 1818910·Product code KWA·September 26, 2012

    ENDEAVOR SPRINT RX

    FDA Adverse Event
    Malfunction ·MEDTRONIC CARIDOVASCULAR GALWAY·Product code NIQ·July 14, 2010

    Heritage Labs Appraise A1c Diabetes Home Test , Product K7609, 24 kits/shipping carton (Product K7609), each kit packed in a box and contains 1 Triad Medium Alcohol Prep Pad, Cat. No. 10-3001, NDC 50730-3001-0, and blood specimen collection supplies, forms, and instructions Blood specimen collection

    FDA Recall
    Terminated ·Heritage Labs International LLC·Product code LCP·January 9, 2011