BEUDAMED
    30 results · 22ms · Sources: EU EUDAMED, US FDA

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    CARDIO 7

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    AGXO

    FDA UDI
    Oticon A/S·05707131233967·K50, BTE 13 CBE AGXO

    2870 3WAY SLIDE VALVE

    FDA UDI
    HANS RUDOLPH, INC.·00817136021027·2870/CLRA/2700 1.375 W/FELR CP

    Pilot Spinal System

    FDA UDI
    Life Spine, Inc.·00190837051365·Pilot Driver, X-Connector

    MINIME NASAL MASK, MODEL P/N 50220

    FDA 510(k)
    FDA Class 2 ·Anesthesiology

    SOUND SURGICAL VASER 2.1 LIPO SYSTEM

    FDA 510(k)
    FDA Class 2 ·General, Plastic Surgery

    EQUINOXE

    FDA Adverse Event
    Injury ·EXACTECH, INC.·Product code KWT·September 13, 2019

    EQUINOXE

    FDA Adverse Event
    Injury ·EXACTECH, INC.·Product code KWT·February 6, 2019

    EON MINI

    FDA Adverse Event
    Malfunction ·ST. JUDE MEDICAL - NEUROMODULATION·Product code LGW·April 26, 2013

    ENDOSCOPIC BILIARY CATHETER

    FDA Adverse Event
    Malfunction ·BOSTON SCIENTIFIC - SPENCER·Product code LQR·June 3, 2011

    CAPD DISCONNECT Y-SET, BULKPACK DISPOSABLE

    FDA Adverse Event
    Malfunction ·BAXTER HEALTHCARE CORPORATION·Product code KDJ·August 12, 2008

    EQUINOXE

    FDA Adverse Event
    Injury ·EXACTECH, INC.·Product code KWT·November 3, 2021

    EQUINOXE

    FDA Adverse Event
    Injury ·EXACTECH, INC.·Product code KWT·July 29, 2019

    EQUINOXE

    FDA Adverse Event
    Injury ·EXACTECH, INC.·Product code KWT·December 26, 2019

    VASERLIPO SYSTEM

    FDA Adverse Event
    Injury ·SOLTA MEDICAL, INC·Product code QPB·January 9, 2023

    EQUINOXE

    FDA Adverse Event
    Injury ·EXACTECH, INC.·Product code KWT·March 4, 2020

    U BY KOTEX SLEEK

    FDA Adverse Event
    Malfunction ·K-C AFC MANUFACTURING, S. DE R.L. DE C.V·Product code HEB·August 31, 2018

    EQUINOXE

    FDA Adverse Event
    Injury ·EXACTECH, INC.·Product code KWT·May 31, 2019

    VASERLIPO SYSTEM

    FDA Adverse Event
    Injury ·SOLTA MEDICAL, INC·Product code QPB·January 5, 2023

    U BY KOTEX SLEEK

    FDA Adverse Event
    Malfunction ·K-C AFC MANUFACTURING, S. DE R.L. DE C.V·Product code HEB·June 27, 2018