BEUDAMED
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    Home Uterine Activity Monitor

    FDA Pre-Market Approval
    FDA Class 2 ·CAREFONE(TM)HOME UTERINE ACTIVITY MONITOR SYSTEM

    Tecomet

    FDA UDI
    TECOMET INC.·00841435108189·MULTIGRASPER

    DeRoyal

    FDA UDI
    DEROYAL INDUSTRIES, INC.·00749756980388·TOTAL HIP PACK

    Anatomic abutment H4mm L6 wide

    FDA UDI
    T.A.G MEDICAL PRODUCTS AGRICULTURAL COOPERATIVE ASSOCIATION·10810190011246·

    Equator Attachment Cap Standard Clear

    FDA UDI
    NOGA MEDICAL PRODUCTS LTD·07290118143451·Equator Attachment Cap Standard Clear

    Anatomic Abutment H4mm L6mm Wide

    FDA UDI
    NOGA MEDICAL PRODUCTS LTD·07290118141723·Anatomic Abutment H4mm L6mm Wide

    FORTIFY ASSURA DR ICD, US

    FDA Adverse Event
    Malfunction ·ST. JUDE MEDICAL, INC.(CRM-SUNNYVALE)·Product code LWS·June 13, 2016

    FORTIFY ASSURA VR ICD_IDE_US

    FDA Adverse Event
    Injury ·ST. JUDE MEDICAL, INC.(CRM-SUNNYVALE)·Product code LWS·March 29, 2017

    ELLIPSE VR ICD

    FDA Adverse Event
    Injury ·ST. JUDE MEDICAL, INC.(CRM-SUNNYVALE)·Product code LWS·March 29, 2017

    CD2257-40Q FORTIFY ASSURA DR ICD_IDE_US

    FDA Adverse Event
    Injury ·ST. JUDE MEDICAL, INC.(CRM-SUNNYVALE)·Product code NVZ·June 14, 2017

    FORTIFY ASSURA VR ICD_IDE_US

    FDA Adverse Event
    Injury ·ST. JUDE MEDICAL, INC.·Product code NVZ·October 31, 2017

    UNIFY ASSURA CRT-D RF HV

    FDA Adverse Event
    Malfunction ·ST. JUDE MEDICAL, INC.(CRM-SYLMAR)·Product code LWS·March 29, 2019

    ENDOPATH* XCEL TROCAR

    FDA Adverse Event
    Malfunction ·ETHICON ENDO SURGERY, INC (CINCINNATI)·Product code GCJ·November 30, 2010

    PULSE GEN MODEL 103

    FDA Adverse Event
    Injury ·CYBERONICS, INC.·Product code LYJ·July 2, 2014

    GOBED+

    FDA Adverse Event
    Malfunction ·STRYKER MEDICAL·Product code FNL·December 19, 2012

    FORTIFY ST DR, U1.6 SJ4 ID

    FDA Adverse Event
    Injury ·ST. JUDE MEDICAL, INC.·Product code LWS·January 18, 2017

    FORTIFYASSURA DR

    FDA Adverse Event
    Injury ·ST. JUDE MEDICAL, INC.(CRM-SUNNYVALE)·Product code LWS·January 3, 2017

    FORTIFY ASSURA VR ICD_O_US

    FDA Adverse Event
    Injury ·ST. JUDE MEDICAL, INC.(CRM-SUNNYVALE)·Product code LWS·January 27, 2016

    STEALTHSTATION¿ S8 SYSTEM

    FDA Adverse Event
    Malfunction ·MEDTRONIC NAVIGATION, INC·Product code HAW·October 10, 2023

    CONTOUR II V-185 AC SERIES TIERED THERAPY DEFIB

    FDA Adverse Event
    Injury ·ST. JUDE MEDICAL, INC.·Product code LWS·November 26, 1999