BEUDAMED
    12 results · 29ms · Sources: EU EUDAMED, US FDA

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    DSL ACTIVE ANDROSTENEDIONE RIA (DSL #3800)

    FDA 510(k)
    FDA Class 1 ·Clinical Chemistry

    DENTAL ACRYLIC POLYMERS

    FDA 510(k)
    FDA Class 2 ·Dental

    DR-2C

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    QUADRA ASSURA CRT-D, DF-4 CONNECTOR

    FDA Adverse Event
    Malfunction ·ST. JUDE MEDICAL, INC., CRMD·Product code NIK·June 6, 2014

    SET, ADMINISTRATION, FOR PERITONEAL DIALYSIS, DISPOSABLE

    FDA Adverse Event
    Injury ·BAXTER HEALTHCARE·Product code KDJ·December 3, 2012

    INRATIO

    FDA Adverse Event
    Other ·ALERE SAN DIEGO, INC.·Product code GJS·September 30, 2010

    COCR TROCH CABLE 2.0MMX750MM

    FDA Adverse Event
    Injury ·ZIMMER BIOMET, INC.·Product code JDQ·August 31, 2018

    ARCOS TROCH CLAW SMALL 100MM

    FDA Adverse Event
    Injury ·ZIMMER BIOMET, INC.·Product code KWA·August 31, 2018

    COCR CABLE/SLEEVE SET 2.0MM

    FDA Adverse Event
    Injury ·ZIMMER BIOMET, INC.·Product code JDQ·August 31, 2018

    32MM COCR BIOMET FEM HD +3 NK

    FDA Adverse Event
    Injury ·BIOMET UK LTD.·Product code KWY·September 7, 2018

    ARCOS CON SZ C STD 80MM HA

    FDA Adverse Event
    Injury ·ZIMMER BIOMET, INC.·Product code KWA·March 7, 2018

    ARCOS 18X190MM SPL TPR DIST HA

    FDA Adverse Event
    Injury ·ZIMMER BIOMET, INC.·Product code LPH·March 7, 2018