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

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    Filters Regulation: Us FDA ×

    Voluson E6, Voluson E8, Voluson E10

    FDA 510(k)
    FDA Class 2 ·Radiology

    SULTAN TOOTH ROOT DESENSITIZER

    FDA 510(k)
    FDA Class 2 ·Dental

    KEYPATH(TM) MRSA/MSSA BLOOD CULTURE TEST- BT

    FDA 510(k)
    FDA Class 1 ·Microbiology

    GMK-HINGE FEMORAL COMPONENT SIZE 3 R

    FDA Adverse Event
    Injury ·MEDACTA INTERNATIONAL SA·Product code KRO·July 25, 2022

    TRILOGY 202

    FDA Adverse Event
    Malfunction ·RESPIRONICS INC.·Product code CBK·June 5, 2013

    ENTERRA

    FDA Adverse Event
    Injury ·MEDTRONIC PUERTO RICO OPERATIONS CO., JUNCOS·Product code LNQ·June 23, 2011

    POWERSAIL CORONARY DILATATION CATHETER

    FDA Adverse Event
    Malfunction ·ABBOTT VASCULAR-CARDIAC THERAPIES·Product code LOX·September 19, 2008

    FLEXI SEAL SIGNAL (FMS)

    FDA Adverse Event
    Injury ·CONVATEC INC.·Product code KNT·October 11, 2016

    XVWEB

    FDA Adverse Event
    Injury ·PLANET DDS·Product code LLZ·March 13, 2025

    SECOND OPINION

    FDA Adverse Event
    Injury ·PEARL INC.·Product code MYN·March 13, 2025