BEUDAMED
    11 results · 21ms · Sources: EU EUDAMED, US FDA

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    SWABBABLE CAP, MODEL 60205

    FDA 510(k)
    FDA Class 2 ·General Hospital

    INRATIO

    FDA Adverse Event
    Malfunction ·HEMOSENSE, INC.·Product code JPA·September 25, 2007

    VERTE-STACK ANATOMIC PEEK STRUT

    FDA Adverse Event
    Injury ·MEDTRONIC SOFAMOR DANEK USA, INC.·Product code MQP·May 5, 2020

    PM 2002 PROLINE/AEC

    FDA 510(k)
    FDA Class 2 ·Dental

    ASEPTICO VCT VERSATILE COMMAND TECHNOLOGY MODEL AEU-925

    FDA 510(k)
    FDA Class 1 ·Dental

    INRATIO

    FDA Adverse Event
    Malfunction ·HEMOSENSE, INC.·Product code JPA·August 20, 2007

    INRATIO

    FDA Adverse Event
    Malfunction ·HEMOSENSE, INC.·Product code JPA·August 27, 2007

    HEARTSTART FRX

    FDA Adverse Event
    Malfunction ·PHILIPS MEDICAL SYSTEMS·Product code MKJ·April 15, 2013

    UNKNOWN DEPUY OVAL DOME PATELLA

    FDA Adverse Event
    Injury ·DEPUY ORTHOPAEDICS, INC.·Product code HTG·April 25, 2011

    COAGUCHEK S SYSTEM

    FDA Adverse Event
    Malfunction ·ROCHE DIAGNOSTICS·Product code JPA·July 3, 2008

    INRATIO

    FDA Adverse Event
    Malfunction ·HEMOSENSE, INC.·Product code JPA·July 27, 2007