BEUDAMED
    7 results · 27ms · Sources: EU EUDAMED, US FDA

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    MONITOR, CARDIAC, BEDSIDE

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    VARI-LASE WIRE FIBER

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

    AMPLIFIER, PHOTOPULSE, MODEL PA13

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    DENTO-SURG 90 F.F.P.F EMC

    FDA Adverse Event
    Other ·ELLMAN INTERNATIONAL·Product code EKZ·March 26, 2014

    GYNECARE GYNEMESH* PS

    FDA Adverse Event
    Injury ·ETHICON, INC.·Product code FTL·October 4, 2012

    ASR ACETABULAR IMPLANT 52

    FDA Adverse Event
    Injury ·DEPUY INTERNATIONAL, LTD.·Product code KWA·July 23, 2010

    ACCOLADE SR SL MRI (Model L310)

    FDA Enforcement
    Class I ·Ongoing·Boston Scientific Corporation·October 22, 2025