BEUDAMED
    11 results · 22ms · Sources: EU EUDAMED, US FDA

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    Filters Regulation: Us FDA ×

    Cercon

    FDA 510(k)
    FDA Class 2 ·Dental

    MIDDLE WHEEL DRIVE POWER CHAIR, CWD01

    FDA 510(k)
    FDA Class 2 ·Physical Medicine

    MESO WOUND MATRIX

    FDA 510(k)
    FDA Unclassified ·Unknown

    COLLEAGUE PRE P1.7

    FDA Adverse Event
    Malfunction ·BAXTER HEALTHCARE - SINGAPORE·Product code FRN·July 15, 2011

    PAINSMART IOD

    FDA Adverse Event
    Malfunction ·MOOG DEVICE GROUP·Product code FRN·May 13, 2013

    SPRINT QUATTRO SECURE

    FDA Adverse Event
    Malfunction ·MPRI·Product code LWS·October 10, 2014

    UNK CHPV

    FDA Adverse Event
    Injury ·Product code JXG·October 19, 2016

    DEKA MOTUS AX

    FDA Adverse Event
    Injury ·EL.EN. ELECTRONIC ENGINEERING S.P.A.·Product code GEX·October 25, 2018

    DEKA MOTUS AX

    FDA Adverse Event
    Malfunction ·EL.EN. ELECTRONIC ENGINEERING S.P.A.·Product code GEX·March 9, 2023

    SKINTACT

    FDA Adverse Event
    Injury ·LEONHARD LANG GMBH·Product code GEI·January 25, 2022

    DEKA MOTUS AX

    FDA Adverse Event
    Malfunction ·EL.EN. ELECTRONIC ENGINEERING S.P.A.·Product code GEX·February 6, 2024