BEUDAMED
    7 results · 20ms · Sources: EU EUDAMED, US FDA

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    NIDEK CV-4000

    FDA 510(k)
    FDA Class 2 ·Ophthalmic

    Klassic HD® Hip System

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    ONCENTRA GYN

    FDA 510(k)
    FDA Class 2 ·Radiology

    HUDSON NEONATAL VENTILATOR CIRCUIT, DUAL LIMB

    FDA Adverse Event
    Malfunction ·TELEFLEX MEDICAL·Product code BZO·October 4, 2010

    QUADRA ASSURA CRT-D, DF-4 CONNECTOR

    FDA Adverse Event
    Malfunction ·ST. JUDE MEDICAL INC., CARDIAC RHYTHM MANAGEMENT D·Product code NIK·January 13, 2014

    ACRYSOF

    FDA Adverse Event
    Injury ·ALCON RESEARCH, LTD. / HUNTINGTON·Product code HQL·December 14, 2012

    SPRYSTEP VECTOR, Custom made device dynamic ankle-foot orthosis (AFO) , Reference numbers: 17V1030, 17V2030, 17V1031, 17V2031, 17V1032, 17V2032, 17V1033, 17V2033, 17V1035, 17V2035, 17V1036, 17V2036, 17V1037, 17V2037

    FDA Enforcement
    Class II ·Completed·Townsend Design·January 17, 2024