BEUDAMED
    10 results · 27ms · Sources: EU EUDAMED, US FDA

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    FDA 510(k)
    FDA Class 1 ·Dental

    Beyes

    FDA UDI
    Beyes Dental Canada Inc·00990010301177·Midwest Type -FG, Trimming and Finishing - 1931

    MOD 427

    FDA 510(k)
    FDA Class 2 ·Radiology

    OMIKRON PACEMAKER 837 UNIPOLAR & 838 BIPOLAR

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    ATTUNE FB TIB BASE SZ 5 CEM

    FDA Adverse Event
    Injury ·DEPUY ORTHOPAEDICS, INC. 1818910·Product code JWH·March 19, 2018

    SHELL WITH CLUSTER HOLES POROUS 52 MM

    FDA Adverse Event
    Injury ·ZIMMER BIOMET, INC.·Product code JDI·January 16, 2019

    STYLE 68 SALINE FILLED BREAST IMPLANT

    FDA Adverse Event
    Injury ·ALLERGAN (COSTA RICA)·Product code FWM·February 23, 2021

    HELIX BLADE 85MM

    FDA Adverse Event
    Injury ·SYNTHES (USA)·Product code JDO·June 19, 2014

    COLLEAGUE CX TRIPLE CHANNEL VOLUMETRIC INFUSION PUMP

    FDA Adverse Event
    Malfunction ·BAXTER HEALTHCARE - SINGAPORE·Product code FRN·October 27, 2010

    CARPENTIER-EDWARDS PERIMOUNT RSR PERICARDIAL BIOPROSTHESIS

    FDA Adverse Event
    Injury ·EDWARDS LIFESCIENCES·Product code DYE·December 21, 2012