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

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    EPI-FOAM SILICONE SHEETING

    FDA 510(k)
    FDA Class 1 ·General, Plastic Surgery

    BA KIT,WE,P37,INL,1',BE,P37,INL,6',STKR

    FDA UDI
    CURBELL MEDICAL PRODUCTS, INC.·00840828136808·BA KIT,WE,P37,INL,1',BE,P37,INL,6',STKR

    CD 3700 SL

    FDA Adverse Event
    Malfunction ·ABBOTT DIAGNOSTICS DIVISION/CELLDYN·Product code GKZ·May 23, 2007

    THE CEN-SLIDE(TM) CENTRIFUGE TUBE

    FDA 510(k)
    FDA Class 1 ·Pathology

    MDPHONE CELLULAR + RESCUE (DEFIB SYSTEM)

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    CELL-DYN 3700 SL ANALYZER

    FDA Adverse Event
    Malfunction ·ABBOTT DIAGNOSTICS DIVISION·Product code GKZ·February 22, 2019

    LIGACLIP** ENDOSCOPIC CLIP APPLIER

    FDA Adverse Event
    Injury ·ETHICON ENDO-SURGERY, LLC.·Product code FZP·March 6, 2013

    ATTAIN OTW

    FDA Adverse Event
    Malfunction ·MEDTRONIC PUERTO RICO, INC.·Product code DTB·February 15, 2011

    CONSULTA CRT-D

    FDA Adverse Event
    Injury ·MEDTRONIC MED REL MEDTRONIC PUERTO RICO·Product code NIK·August 8, 2014