BEUDAMED
    13 results · 24ms · Sources: EU EUDAMED, US FDA

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    AST (UV) TEST

    FDA 510(k)
    FDA Class 2 ·Clinical Chemistry

    ETG 255 COMBO STIMUALTOR, TEN 260 STIMUALTOR

    FDA 510(k)
    FDA Class 2 ·Neurology

    ACIST ANGIOGRAPHIC INJECTION SYSTEM, MODEL R2000-CMS

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    ACIST

    FDA Adverse Event
    Injury ·ACIST MEDICAL SYSTEMS, INC.·Product code DXT·February 10, 2012

    GMK-SPHERE TIBIAL INSERT FIXED FLEX SIZE 3/10 MM R

    FDA Adverse Event
    Injury ·MEDACTA INTERNATIONAL SA·Product code JWH·November 17, 2020

    SYNERGY

    FDA Adverse Event
    Injury ·MDT SOFAMOR DANEK PUERTO RICO MFG·Product code LGW·May 14, 2014

    MAXIMO II CRT-D

    FDA Adverse Event
    Injury ·MEDTRONIC MED REL, INC.·Product code NIK·October 31, 2012

    AMPLATZER TORQVUE DELIVERY SYSTEM

    FDA Adverse Event
    Malfunction ·AGA MEDICAL CORPORATION·Product code DQY·August 20, 2010

    ACIST

    FDA Adverse Event
    Malfunction ·ACIST MEDICAL SYSTEMS, INC.·Product code DXT·April 20, 2007

    ACIST

    FDA Adverse Event
    Injury ·ACIST MEDICAL SYSTEMS, INC.·Product code DXT·February 10, 2012

    GALAXY G3 6MM X 15CM

    FDA Adverse Event
    Injury ·MEDOS INTERNATIONAL SARL·Product code KRD·January 17, 2023

    GALAXY G3 XSFT 3MM X 6CM

    FDA Adverse Event
    Injury ·MEDOS INTERNATIONAL SARL·Product code KRD·January 17, 2023

    GALAXY G3 4MM X 12CM

    FDA Adverse Event
    Injury ·MEDOS INTERNATIONAL SARL·Product code KRD·January 17, 2023