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

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    CRYOPATCH SG PULMONARY HUMAN CARDIAC PATCH

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    Mesh|Ex

    FDA UDI
    EXSURCO MEDICAL, INC.·00810006780192·ASM, Cutting Roller C

    MicroScan

    FDA UDI
    Beckman Coulter, Inc.·15099590658953·MicroScan Turbidity Meter

    PEAK MEDICAL

    FDA UDI
    Peak Medical Distribution Inc.·G45333151018660·DOUBLE ENDED V-BLADE HEAVY DUTY LENGTH ADJUSTAB...

    OXYHEAL 2000 HYPERBARIC CHAMBER SERIES, MODEL OXYHEAL 2000 SERIES

    FDA 510(k)
    FDA Class 2 ·Anesthesiology

    TCM400

    FDA 510(k)
    FDA Class 2 ·Anesthesiology

    Widex

    FDA UDI
    Widex A/S·05706069727128·Widex EVOKE E-PA (Autumn Beige S-110 ) RC coil

    BD BBL¿ THIOGLYCOLLATE MEDIUM, ENRICHED WITH VITAMIN K1 AND HEMIN

    FDA Adverse Event
    Malfunction ·BECTON, DICKINSON & CO.·Product code JSG·August 22, 2019

    KYPHOPAK TRAY

    FDA Adverse Event
    Malfunction ·MDT KYPHON NEUCHATEL MFG·Product code HRX·May 24, 2021

    KYPHON XPANDER II INFLATABLE BONE TAMP

    FDA Adverse Event
    Malfunction ·MEDTRONIC MEXICO·Product code HRX·November 6, 2019

    KYPHON XPANDER II INFLATABLE BONE TAMP

    FDA Adverse Event
    Malfunction ·MEDTRONIC MEXICO·Product code HRX·April 5, 2021

    KYPHON XPANDER II INFLATABLE BONE TAMP

    FDA Adverse Event
    Malfunction ·MEDTRONIC MEXICO·Product code HRX·July 11, 2019

    KYPHON XPANDER II INFLATABLE BONE TAMP

    FDA Adverse Event
    Malfunction ·MEDTRONIC MEXICO·Product code HRX·August 31, 2019

    KYPHON XPANDER II INFLATABLE BONE TAMP

    FDA Adverse Event
    Malfunction ·MDT KYPHON NEUCHATEL MFG·Product code HRX·March 7, 2018

    S-ICD SYSTEM

    FDA Adverse Event
    Malfunction ·CAMERON HEALTH·Product code LWS·May 3, 2013

    SAGITTAL BLADE

    FDA Adverse Event
    Malfunction ·STRYKER IRELAND LTD.·Product code GFA·April 29, 2011

    INTERSTIM

    FDA Adverse Event
    Injury ·MEDTRONIC PUERTO RICO OPERATIONS CO.·Product code EZW·August 7, 2008

    KYPHON XPANDER II INFLATABLE BONE TAMP

    FDA Adverse Event
    Malfunction ·MEDTRONIC SOFAMOR DANEK·Product code HRX·May 17, 2018

    1030489-2019-01511

    FDA Adverse Event
    Death ·MEDTRONIC SOFAMOR DANEK USA, INC.·Product code NDN·December 31, 2019

    KYPHON XPANDER

    FDA Adverse Event
    Malfunction ·MEDTRONIC MEXICO·Product code HRX·March 23, 2021