BEUDAMED
    13 results · 19ms · Sources: EU EUDAMED, US FDA

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    COMPONENTS FOR CARDIOVASCULAR PROCEDURE KIT

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    ACDF STAND ALONE CERVICAL

    FDA Adverse Event
    Injury ·MEDACTA INTERNATIONAL SA·Product code OVE·October 8, 2025

    VERIFY BIOLOGICAL INDICATOR CHALLENGE PACK FOR VAPORIZED VH202 STERILIZATION

    FDA 510(k)
    FDA Class 2 ·General Hospital

    Mecta-C Stand Alone

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    ACDF STAND ALONE CERVICAL

    FDA Adverse Event
    Injury ·MEDACTA INTERNATIONAL SA·Product code OVE·April 25, 2025

    OCTRODE

    FDA Adverse Event
    Injury ·ST. JUDE MEDICAL - NEUROMODULATION·Product code GZB·November 5, 2014

    ACDF STAND ALONE CERVICAL

    FDA Adverse Event
    Injury ·MEDACTA INTERNATIONAL SA·Product code OVE·December 22, 2025

    RENEW RECEIVER KIT, 16-CHANNEL

    FDA Adverse Event
    Injury ·ST. JUDE MEDICAL - NEUROMODULATION·Product code GZB·February 4, 2015

    MALLINCKRODT

    FDA Adverse Event
    Malfunction ·COVIDIEN, FORMERLY TYCOHEALTH·Product code BTS·February 28, 2013

    6600

    FDA Adverse Event
    Malfunction ·GE OEC MEDICAL SYSTEMS (SLC)·Product code JAA·February 5, 2011

    CAPSUREFIX

    FDA Adverse Event
    Injury ·MPRI·Product code DTB·August 8, 2014

    ACDF 03.18.118 MECTA-C SA TIPEEK CAGE 18X15X6X7°

    FDA Adverse Event
    Injury ·MEDACTA INTERNATIONAL SA·Product code OVE·May 12, 2023

    ACDF STAND ALONE CERVICAL

    FDA Adverse Event
    Malfunction ·MEDACTA INTERNATIONAL SA·Product code OVE·June 13, 2025