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

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    ASCENSION MUH

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    Wireless microphone package

    FDA UDI
    Shenzhen Mindray Bio-Medical Electronics Co., Ltd.·06936415927806·

    PRECISE RX NITINOL STENT TRANSHEPATIC BILIARY SYSTEM

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

    CATHCOR DESKTOP

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    CD HORIZON SPINAL SYSTEM

    FDA Adverse Event
    Injury ·WARSAW ORTHOPEDICS·Product code KWP·September 16, 2016

    LIFESTENT VALEO BILIARY STENT

    FDA Adverse Event
    Malfunction ·BARD PERIPHERAL VASCULAR, INC.·Product code FGE·December 29, 2009

    CD HORIZON SPINAL SYSTEM

    FDA Adverse Event
    Malfunction ·WARSAW ORTHOPAEDIC INC.·Product code KWP·June 25, 2009

    CD HORIZON SPINAL SYSTEM

    FDA Adverse Event
    Malfunction ·WARSAW ORTHOPEDIC INC.·Product code KWQ·July 23, 2009

    CD HORIZON SPINAL SYSTEM

    FDA Adverse Event
    Injury ·MEDTRONIC SOFAMOR DANEK·Product code KWP·August 30, 2013

    CD HORIZON SPINAL SYSTEM

    FDA Adverse Event
    Injury ·WARSAW ORTHOPEDICS·Product code KWP·September 16, 2016

    CD HORIZON SPINAL SYSTEM

    FDA Adverse Event
    Injury ·WARSAW ORTHOPEDICS·Product code KWP·December 23, 2011

    LIFESTENT VALEO BILIARY STENT

    FDA Adverse Event
    Malfunction ·BARD PERIPHERAL VASCULAR, INC.·Product code FGE·December 29, 2009

    CD HORIZON ADANTA

    FDA Adverse Event
    Other ·MEDTRONIC SOFAMOR DANEK·Product code KWP·April 3, 2009

    LIFESTENT VALEO VASCULAR STENT

    FDA Adverse Event
    Injury ·BARD PERIPHERAL VASCULAR, INC.·Product code FGE·August 9, 2010

    DEXCOM G7 CONTINUOUS GLUCOSE MONITORING SYSTEM

    FDA Adverse Event
    Malfunction ·DEXCOM, INC.·Product code QBJ·March 9, 2023

    CD HORIZON SPINAL SYSTEM

    FDA Adverse Event
    Malfunction ·MEDTRONIC SOFAMOR DANEK PUERTO RICO OPER·Product code KWP·June 10, 2009

    INSERTER FOR TI ELASTIC NAILS

    FDA Adverse Event
    Malfunction ·SYNTHES GMBH·Product code LXH·April 11, 2013

    HEARTMATE II SYSTEM CONTROLLER

    FDA Adverse Event
    Malfunction ·THORATEC CORP.·Product code DSQ·March 1, 2011

    NIHON KOHDEN NE-136A ELECTRODE

    FDA Adverse Event
    Injury ·NIHON KOHDEN CORPORATION·Product code GWQ·May 23, 2008

    CD HORIZON SPINAL SYSTEM

    FDA Adverse Event
    Malfunction ·MEDTRONIC SOFAMOR DANEK·Product code KWP·March 26, 2010