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

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    INTERTAN CHS LIMITED COLLAPSE SET SCREW

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    ENVAN HEART RATE MONITOR

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    EMBRYON GIFT TRANSFER CATHETERS/SETS

    FDA 510(k)
    FDA Class 2 ·Obstetrics/Gynecology

    SET, ADMINISTRATION, FOR PERITONEAL DIALYSIS, DISPOSABLE

    FDA Adverse Event
    Injury ·BAXTER HEALTHCARE·Product code KDJ·May 2, 2013

    AMS ELEVATE POSTERIOR PROLAPSE REPAIR SYSTEM WITH INTEPRO LITE

    FDA Adverse Event
    Injury ·AMERICAN MEDICAL SYSTEMS (MN)·Product code OTP·September 15, 2014

    E SERIES DEFIBRILLATOR

    FDA Adverse Event
    Malfunction ·ZOLL MEDICAL CORPORATION·Product code MKJ·April 19, 2011

    AVAN REINF RING SS 48/58MM

    FDA Adverse Event
    Injury ·BIOMET UK LTD.·Product code LZO·December 29, 2025