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

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    DOMAIN SURGICAL SYSTEM

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

    VIRTUE MALE SLING SYSTEM AND ALEXIS(R) WOUND RETRACTOR KIT

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

    ENDIUS TITLE SPINAL FIXATION SYSTEM

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    ALARIS SYSTEM

    FDA Adverse Event
    Malfunction ·CAREFUSION SD·Product code FRN·October 15, 2025

    ALIGN TO URETHRAL SUPPORT SYSTEM

    FDA Adverse Event
    Injury ·C.R. BARD, INC. (COVINGTON) -1018233·Product code OTN·May 15, 2013

    EDWARDS SAPIEN XT TRANSCATHETER HEART VALVE

    FDA Adverse Event
    Injury ·EDWARDS LIFESCIENCES·Product code NPT·September 26, 2014

    TRANSSEPTAL NEEDLE, BRK SERIES, ADULT 18 GA, 71CM

    FDA Adverse Event
    Malfunction ·ST. JUDE MEDICAL, AF DIVISION·Product code DRC·May 23, 2011

    EA DELTA CER INSERT 36IDX52OD

    FDA Adverse Event
    Malfunction ·DEPUY ORTHOPAEDICS INC US·Product code LZO·March 4, 2021

    EA DELTA CER INSERT 36IDX52OD

    FDA Adverse Event
    Malfunction ·DEPUY ORTHOPAEDICS, INC. 1818910·Product code MRA·July 1, 2019

    DELTA CER INSERT 36ID X 56OD

    FDA Adverse Event
    Malfunction ·DEPUY IRELAND 9616671·Product code MRA·September 2, 2015

    EA DELTA CER INSERT 36IDX52OD

    FDA Adverse Event
    Malfunction ·DEPUY ORTHOPAEDICS INC US·Product code KWA·March 13, 2018

    EA DELTA CER INSERT 36IDX52OD

    FDA Adverse Event
    Injury ·DEPUY ORTHOPAEDICS, INC. 1818910 ·Product code LZO·February 22, 2018