BEUDAMED
    769 results · 49ms · Sources: EU EUDAMED, US FDA

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    PRO-PROJECT

    FDA registration
    PRO-PROJECT·1 product·🇵🇱 Poland

    PRO-JECT(TM) SAFETY NEEDLE HOLDER

    FDA 510(k)
    FDA Class 2 ·Clinical Chemistry

    WATCHMAN FLX PRO LAA CLOSURE DEVICE WITH DELIVERY SYSTEM

    FDA Adverse Event
    Injury ·BOSTON SCIENTIFIC CORPORATION·Product code NGV·December 20, 2023

    MEDTRONIC TRANSCATHETER VALVE

    FDA Adverse Event
    Injury ·MEDTRONIC HEART VALVES DIVISION·Product code NPT·July 12, 2022

    CENTRELLA PRO+ 36"

    FDA Adverse Event
    Malfunction ·HILL-ROLM INC / HILL-ROM, INC.·Product code IOQ·May 29, 2024

    CRE PRO

    FDA Adverse Event
    Malfunction ·BOSTON SCIENTIFIC CORPORATION·Product code FGE·June 27, 2023

    IMPLANTABLE PACEMAKER PULSE-GENERATOR

    FDA Adverse Event
    Malfunction ·BOSTON SCIENTIFIC CORPORATION·Product code DXY·December 1, 2022

    DURACELL PRO

    FDA Adverse Event
    Malfunction ·*·Product code FCO·February 6, 2004

    S8 STEALTHSTATION NAVIGATION SYSTEM

    FDA Adverse Event
    Malfunction ·MEDTRONIC NAVIGATION, INC·Product code HAW·November 13, 2018

    PRO-VENT PLUS ARTERIAL BLOOD SAMPLING KIT

    FDA Adverse Event
    Malfunction ·SMITHS MEDICAL ASD, INC.·Product code CBT·September 8, 2006

    MEDTRONIC TRANSCATHETER VALVE

    FDA Adverse Event
    Injury ·MEDTRONIC HEART VALVES DIVISION·Product code NPT·December 11, 2023

    MOSAIC AORTIC BIOPROSTHETIC HEART VALVE

    FDA Adverse Event
    Injury ·MEDTRONIC HEART VALVES DIVISION·Product code DYE·February 7, 2024

    VENFLON PRO SAFETY 20GA 1.1MM OD 32MM L

    FDA Adverse Event
    Malfunction ·BECTON DICKINSON MEDICAL (SINGAPORE)·Product code FOZ·November 21, 2019

    PRO-VENT(TM), PULSATOR(R), AND LINE DRAW

    FDA Adverse Event
    Malfunction ·SMITHS MEDICAL ASD, INC.·Product code JKA·August 31, 2022

    SC UPMD SET

    FDA Adverse Event
    Malfunction ·B.BRAUN SURGICAL SA·Product code GAT·June 12, 2018

    ESSURE

    FDA Adverse Event
    Injury ·BAYER PHARMA AG·Product code HHS·May 25, 2021

    JELCO® HYPODERMIC NEEDLE-PRO® DEVICE

    FDA Adverse Event
    Malfunction ·SMITHS MEDICAL ASD, INC.·Product code FMI·July 31, 2017

    NAVITOR TRANSCATHETER AORTIC VALVE

    FDA Adverse Event
    Injury ·ABBOTT MEDICAL·Product code NPT·July 18, 2025

    BD VENFLON¿ PRO SAFETY SHIELDED IV CATHETER

    FDA Adverse Event
    Malfunction ·BECTON DICKINSON MEDICAL (SINGAPORE)·Product code FOZ·January 6, 2020

    BD VENFLON¿ PRO SAFETY SHIELDED IV CATHETER

    FDA Adverse Event
    Malfunction ·BECTON DICKINSON MEDICAL (SINGAPORE)·Product code FOZ·December 19, 2019