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

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    K-ASSAY FIBRINOGEN

    FDA 510(k)
    FDA Class 2 ·Hematology

    artegral life

    FDA UDI
    Merz Dental GmbH·D7091993482·anteriors; shade D3; mould UCM

    KORN MANDIBULAR ADVANCER

    FDA 510(k)
    FDA Class 1 ·Dental

    PrisMax System Version 3

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

    SPECIFIC DEVICE NOT REPORTED

    FDA Adverse Event
    Injury ·EXACTECH, INC.·Product code JDI·June 18, 2024

    ENVOY 6F GUIDING CATHETERS

    FDA Adverse Event
    Malfunction ·CORDIS DE MEXICO·Product code DQY·March 7, 2013

    PARADIGM REAL-TIME INSULIN INFUSION PUMP

    FDA Adverse Event
    Injury ·MEDTRONIC PUERTO RICO OPERATIONS MED-REL·Product code MDS·February 8, 2011

    ENRHYTHM DR

    FDA Adverse Event
    Injury ·IPG MFG SWITZERLAND·Product code NVZ·August 8, 2014

    ANATOMICAL SHOULDER DOMELOCK, DOME, CENTRIC

    FDA Adverse Event
    Injury ·ZIMMER SWITZERLAND MANUFACTURING GMBH·Product code PHX·June 1, 2023

    ANATOMICAL SHOULDER, HUMERAL STEM, UNCEMENTED, 14, 100 MM

    FDA Adverse Event
    Injury ·ZIMMER SWITZERLAND MANUFACTURING GMBH·Product code PHX·June 1, 2023

    ANATOMICAL SHOULDER DOMELOCK, HUMERAL HEAD, 50-21, R=27.6MM

    FDA Adverse Event
    Injury ·ZIMMER SWITZERLAND MANUFACTURING GMBH·Product code PHX·June 1, 2023