BEUDAMED
    7 results · 17ms · Sources: EU EUDAMED, US FDA

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    MODEL 2000 MONITOR

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    ERA® Implant Abutment Micro Ang. Base, 4mm Cuff (AN)

    FDA UDI
    STERNGOLD DENTAL LLC·00841549104992·Implant retained overdentures are an establishe...

    PORTA SMK 82, MODEL 2032

    FDA 510(k)
    FDA Class 2 ·Dental

    REVIVE INTERMEDIATE CATHETER (REVIVE IC)

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    M2A 1 PC SHELL 38MMX52MM

    FDA Adverse Event
    Injury ·BIOMET ORTHOPEDICS·Product code KWA·May 15, 2014

    CAPSUREFIX NOVUS

    FDA Adverse Event
    Malfunction ·MEDTRONIC PUERTO RICO, INC.·Product code DTB·October 31, 2012

    DEXTRUS 4137

    FDA Adverse Event
    Malfunction ·BIOTRONIK SE & CO. KG·Product code NVZ·August 11, 2010