BEUDAMED
    9 results · 28ms · Sources: EU EUDAMED, US FDA

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    Filters Regulation: Us FDA ×

    ARIX Ankle Distal Tibia System

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    ELMED

    FDA UDI
    ELMED INCORPORATED·00842180148307·Burgess Carpal Tunnel Retractor, Overall Length...

    TROJAN JAGUAR MALE NATURAL RUBBER LATEX CONDOM WITH WARMING AND TINGLING LUBRICANT

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

    VS Newborn Heart Rate Monitor

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    PULLUP

    FDA Adverse Event
    Malfunction ·S.B.M. SAS·Product code MBI·April 12, 2023

    TEXIUM

    FDA Adverse Event
    Malfunction ·SISTEMAS MEDICOS ALARIS S.A DE C.V.·Product code FMF·March 19, 2026

    SET, ADMINISTRATION, FOR PERITONEAL DIALYSIS, DISPOSABLE

    FDA Adverse Event
    Injury ·BAXTER HEALTHCARE·Product code KDJ·September 1, 2011

    GRANUFLO

    FDA Adverse Event
    Death ·FRESENIUS MEDICAL CARE NORTH AMERICA·Product code KPO·November 4, 2014

    PLV-100

    FDA Adverse Event
    Malfunction ·RESPIRONICS, INC.·Product code CBK·July 15, 2013