BEUDAMED
    12 results · 26ms · Sources: EU EUDAMED, US FDA

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    CONPHAR CATHETER PLUG

    FDA 510(k)
    FDA Class 1 ·General, Plastic Surgery

    n.a.

    FDA UDI
    Karl Storz GmbH & Co. KG·04048551200056·JAMESON Scissors, 15.5 cm

    Rongeur

    FDA UDI
    KATENA PRODUCTS, INC.·00841668108505·KERRISON RONGEUR SIZE 3

    ACTIVA

    FDA Adverse Event
    Malfunction ·MEDTRONIC MED REL MEDTRONIC PUERTO RICO·Product code MHY·July 8, 2013

    SMARTTRACK SYSTEM

    FDA 510(k)
    FDA Class 2 ·Anesthesiology

    Orthopedic Fixation Pin

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    ACTIVA

    FDA Adverse Event
    Malfunction ·MEDTRONIC MED REL MEDTRONIC PUERTO RICO·Product code MHY·July 22, 2013

    ACTIVA

    FDA Adverse Event
    Injury ·MEDTRONIC MED REL MEDTRONIC PUERTO RICO·Product code MHY·June 29, 2012

    SOLETRA

    FDA Adverse Event
    Injury ·MEDTRONIC MED REL MEDTRONIC PUERTO RICO·Product code MHY·June 29, 2012

    AMS INVANCE MALE SLING SYSTEM

    FDA Adverse Event
    Injury ·AMERICAN MEDICAL SYSTEMS (MN)·Product code HWC·May 6, 2014

    OT VERIO PRO METER

    FDA Adverse Event
    Malfunction ·LIFESCAN EUROPE, A DIVISION OF CILAG GMBH INTL·Product code NBW·October 15, 2012

    PUMP MMT-722NAS PRDGM INS V2.2 SK EN

    FDA Adverse Event
    Injury ·MEDTRONIC PUERTO RICO OPERATIONS MED-REL·Product code LZG·August 4, 2010