BEUDAMED
    42 results · 31ms · Sources: EU EUDAMED, US FDA

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    Vonflex S

    FDA 510(k)
    FDA Class 2 ·Dental

    Collar Popper – Pin

    FDA UDI
    SIGNATURE ORTHOPAEDICS PTY LTD·09348215095949·

    Endo-Model Modular Knee Prosthesis System

    FDA UDI
    WALDEMAR LINK GmbH & Co. KG·04026575419111·Proximal Tibial Spacer,Size x-small, incl. flat...

    Endo-Model Modular Knee Prosthesis System

    FDA UDI
    WALDEMAR LINK GmbH & Co. KG·04026575419104·Proximal Tibial Spacer,Size x-small, incl. flat...

    Endo-Model Modular Knee Prosthesis System

    FDA UDI
    WALDEMAR LINK GmbH & Co. KG·04026575419098·Proximal Tibial Spacer,Size x-small, incl. flat...

    WIRELESS DR IMAGING OPTION-WDR1

    FDA 510(k)
    FDA Class 2 ·Radiology

    MEDISIZE GOLD

    FDA 510(k)
    FDA Class 2 ·Anesthesiology

    OrthoMedFlex

    FDA UDI
    ORTHOMEDFLEX LLC·M7161111526150·Ceramic Femoral Head, 28mm, XXL (+10 mm)

    MINICAP TRANSFER SET

    FDA Adverse Event
    Malfunction ·BAXTER HEALTHCARE CORPORATION·Product code KDJ·December 15, 2020

    MINICAP TRANSFER SET

    FDA Adverse Event
    Malfunction ·BAXTER HEALTHCARE CORPORATION·Product code KDJ·August 24, 2020

    MINICAP TRANSFER SET

    FDA Adverse Event
    Malfunction ·BAXTER HEALTHCARE CORPORATION·Product code KDJ·April 18, 2023

    MINICAP TRANSFER SET

    FDA Adverse Event
    Malfunction ·BAXTER HEALTHCARE CORPORATION·Product code KDJ·January 3, 2024

    LOCKING TITANIUM ADAPTER

    FDA Adverse Event
    Malfunction ·BAXTER HEALTHCARE - SWINFORD·Product code KDJ·April 18, 2018

    ACRYSOF TORIC

    FDA Adverse Event
    Injury ·ALCON RESEARCH, LTD. / HUNTINGTON·Product code HQL·June 5, 2013

    2800

    FDA Adverse Event
    Malfunction ·GE OEC MEDICAL SYSTEMS (SLC)·Product code JAA·June 27, 2011

    SMARTSITE INFUSION SET

    FDA Adverse Event
    Malfunction ·CAREFUSION·Product code FPA·October 2, 2014

    MINICAP TRANSFER SET

    FDA Adverse Event
    Malfunction ·BAXTER HEALTHCARE CORPORATION·Product code KDJ·January 3, 2023

    MINICAP

    FDA Adverse Event
    Malfunction ·BAXTER INTERNATIONAL INC.·Product code KDJ·October 28, 2024

    MINICAP TRANSFER SET

    FDA Adverse Event
    Malfunction ·BAXTER HEALTHCARE CORPORATION·Product code KDJ·February 1, 2021

    MINICAP TRANSFER SET

    FDA Adverse Event
    Malfunction ·BAXTER HEALTHCARE CORPORATION·Product code KDJ·March 23, 2021