BEUDAMED
    33 results · 24ms · Sources: EU EUDAMED, US FDA

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    exGraft, exGraft Carbon

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    ZenFlex CM

    FDA UDI
    Kerr Corporation·00195062145698·.25/.06/21mm ZenFlex CM iTi FILE REFILL PACK

    NORTECH SYSTEMS, INC.

    FDA registration
    NORTECH SYSTEMS, INC.·22 products·🇺🇸 United States

    PULSE-GENERATOR, DUAL CHAMBER, IMPLANTABLE

    FDA Adverse Event
    Malfunction ·MEDTRONIC MILACA, INC.·Product code DTE·April 10, 2013

    QUANTA SYSTEM POLYSURGE DIODE LASER FAMILY

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

    INPECTRA STO2 SPOT CHECK

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    TRUWAVE

    FDA Adverse Event
    Malfunction ·EDWARDS LIFESCIENCES DR·Product code DXO·April 22, 2026

    BIFUSE EXTENTION SET

    FDA Adverse Event
    Malfunction ·ICU MEDICAL, INC.·Product code FMG·March 2, 2017

    2183613-2012-00515

    FDA Adverse Event
    Malfunction ·MEDTRONIC MILACA INC.·Product code DPS·April 11, 2012

    2183613-1997-00011

    FDA Adverse Event
    Injury ·September 10, 1997

    2183613-2010-00026

    FDA Adverse Event
    Malfunction ·MEDTRONIC MILACA, INC.·October 20, 2010

    2183613-2012-01832

    FDA Adverse Event
    Malfunction ·MEDTRONIC MILACA INC.·Product code DPS·October 31, 2012

    2183613-1997-00004

    FDA Adverse Event
    Injury ·March 10, 1997

    2183613-2010-00022

    FDA Adverse Event
    Malfunction ·MEDTRONIC MILACA, INC.·December 15, 2011

    2183613-2010-00028

    FDA Adverse Event
    Malfunction ·MEDTRONIC MILACA, INC.·April 14, 2011

    2183613-2018-00177

    FDA Adverse Event
    Malfunction ·August 3, 2018

    2183613-1999-00011

    FDA Adverse Event
    Injury ·September 8, 1999

    2183613-1999-00013

    FDA Adverse Event
    Injury ·September 8, 1999

    2183613-1999-00012

    FDA Adverse Event
    Malfunction ·September 8, 1999

    2183613-1999-00015

    FDA Adverse Event
    Injury ·September 8, 1999