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

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    ENDOSCOPIC ELECTROSURGICAL INSTRUMENTS AND ELECTRODES

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

    artegral

    FDA UDI
    Merz Dental GmbH·D7091972008·posteriors; shade A1; size XS; upper jaw

    VQ ORTHOCARE

    FDA UDI
    Vision Quest Industries Incorporated·00817717022535·BIONICARE ALIGN PREFAB PB R

    VQ ORTHOCARE

    FDA UDI
    Vision Quest Industries Incorporated·00817717022542·BIONICARE ALIGN PREFAB PB HD R

    ARIX Humerus System

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    BRAEMAR ER900 WIRELESS SERIES ARRHYTHMIA EVENT RECORDER

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    TOTALCARE BED

    FDA Adverse Event
    Malfunction ·HILL-ROM INC.·Product code FNL·January 22, 2013

    CAPSUREFIX

    FDA Adverse Event
    Death ·MEDTRONIC PUERTO RICO, INC.·Product code DTB·January 27, 2011

    530G INSULIN PUMP

    FDA Adverse Event
    Malfunction ·MEDTRONIC PUERTO RICO OPERATIONS CO.·Product code OZO·July 31, 2014

    ONYX

    FDA Adverse Event
    Death ·MICRO THERAPEUTICS, INC. DBA EV3·Product code MFE·October 1, 2024

    MARATHON

    FDA Adverse Event
    Death ·MICRO THERAPEUTICS, INC. DBA EV3·Product code KRA·October 1, 2024

    ONYX

    FDA Adverse Event
    Injury ·MICRO THERAPEUTICS, INC. DBA EV3·Product code MFE·October 1, 2024

    MARATHON

    FDA Adverse Event
    Injury ·MICRO THERAPEUTICS, INC. DBA EV3·Product code KRA·October 1, 2024

    ENDOPATH ENDOSCOPIC ARTICULATING MULTIFEED STAPLER

    FDA Adverse Event
    Malfunction ·ETHICON ENDO-SURGERY, INC.·Product code GAG·April 22, 1997