BEUDAMED
    15 results · 21ms · Sources: EU EUDAMED, US FDA

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    SOZO

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    PRINCETON

    FDA UDI
    Princeton Medical Group, Inc.·00810158214446·UTERINE CURETTE RECAMIER BLUNT RIGID FIG. 1 7MM...

    X8 Locking Driver

    FDA UDI
    SIGNATURE ORTHOPAEDICS PTY LTD·09348215057824·

    INSYTE AUTOG BC WING PNK 20GA X1.16IN

    FDA Adverse Event
    Malfunction ·BECTON DICKINSON·Product code FOZ·December 12, 2024

    AREA-CT, TZ MEDICAL MCOT ECG MONITOR AND ARRHYTHMIA DETECTOR

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    ENDOWAVE INFUSION SYSTEM

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    PUSHING CATHETER

    FDA Adverse Event
    Malfunction ·COOK IRELAND LTD·Product code FGE·October 19, 2022

    ROBOTIC ARM INTERACTIVE ORTHOPEDIC SYSTEM-RIO

    FDA Adverse Event
    Malfunction ·MAKO SURGICAL·Product code OLO·April 25, 2014

    ROBOTIC ARM INTERACTIVE ORTHOPEDIC SYSTEM-RIO

    FDA Adverse Event
    Malfunction ·MAKO SURGICAL·Product code NPJ·April 25, 2014

    MINICAP

    FDA Adverse Event
    Injury ·BAXTER HEALTHCARE - CLEVELAND·Product code KDI·June 17, 2013

    ULTRACISION HARMONIC SCALPEL CURVED SHEARS (LCS)-PISTOL GRIP 36CM - 15MM ACTIVE

    FDA Adverse Event
    Malfunction ·ETHICON ENDO-SURGERY, LLC.·Product code GEI·September 22, 2008

    UNICEL DXI 800 ACCESS IMMUNOASSAY SYSTEM

    FDA Adverse Event
    Malfunction ·BECKMAN COULTER, INC.·Product code JJE·June 24, 2011

    PUSHING CATHETER

    FDA Adverse Event
    Malfunction ·COOK IRELAND LTD·Product code FGE·September 15, 2023

    PUSHING CATHETER

    FDA Adverse Event
    Malfunction ·COOK IRELAND LTD·Product code FCG·June 28, 2023

    PUSHING CATHETER

    FDA Adverse Event
    Malfunction ·COOK IRELAND LTD·Product code FGE·March 5, 2021