BEUDAMED
    9 results · 26ms · Sources: EU EUDAMED, US FDA

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    REGENESIS MODEL 42

    FDA 510(k)
    FDA Class 2 ·Physical Medicine

    artegral

    FDA UDI
    Merz Dental GmbH·D7091972093·posteriors; shade C1; size L; lower jaw

    De Soutter Medical

    FDA UDI
    DE SOUTTER MEDICAL LIMITED·05051471123038·K-WIRE - DOUBLE TROCAR 0.9mm DIA x 75mm

    PRISMAFLEX SYSTEM, VERSION 3.20

    FDA 510(k)
    FDA Class 2 ·Gastroenterology, Urology

    Reprocessed Covidien Trocar

    FDA 510(k)
    FDA Class 2 ·Gastroenterology, Urology

    PRISMAFLEX

    FDA Adverse Event
    Injury ·GAMBRO LUNDIA AB·Product code KDI·October 7, 2010

    AUTOPULSE NIMH BATTERY

    FDA Adverse Event
    Malfunction ·ZOLL CIRCULATION, INC.·Product code DRM·January 22, 2013

    HOMECHOICE AUTOMATED PD SET WITH CASSETTE

    FDA Adverse Event
    Malfunction ·BAXTER HEALTHCARE - MOUNTAIN HOME·Product code FKX·July 31, 2014

    UNICEL® DXC 600I ACCESS® 2 IMMUNOASSAY SYSTEM

    FDA Adverse Event
    Malfunction ·BECKMAN COULTER, INC.·Product code MMI·January 27, 2011