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

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    MALLINCKRODT, GOODKNIGHT 418S

    FDA 510(k)
    FDA Class 2 ·Anesthesiology

    Preat Implant Prosthetics

    FDA UDI
    Preat Corporation·00842092179475·Biomet 3i Certain®-compatible 5.0mm Titanium Sc...

    Custom Procedure Kit

    FDA UDI
    MEDIVATORS INC.·40677964015760·Endo Carry-On Procedure Kit

    PedFuse®

    FDA UDI
    SPINEFRONTIER, INC.·00190361008835·PedFuse Reset, CNL, 5.0mm x 45mm

    MODIFICATION TO JMS A.V. FISTULA NEEDLE SET

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

    SYSMEX AUTOMATED COAGULATION ANALYZER, MODEL CA-6000

    FDA 510(k)
    FDA Class 2 ·Hematology

    CARDIOSAVE HYBRID, 3.1 EDITION

    FDA Adverse Event
    Malfunction ·DATASCOPE CORP. - MAHWAH·Product code DSP·November 14, 2023

    PREMIUM PLUS CEEA

    FDA Adverse Event
    Malfunction ·US SURGICAL PUERTO RICO·Product code GDW·April 19, 2018

    CARDIOSAVE HYBRID, TYPE B PLUG

    FDA Adverse Event
    Malfunction ·DATASCOPE CORP.·Product code DSP·July 22, 2024

    CARDIOSAVE HYBRID, 3.1 EDITION

    FDA Adverse Event
    Malfunction ·DATASCOPE CORP. - MAHWAH·Product code DSP·February 15, 2024

    CARDIOSAVE HYBRID, TYPE B PLUG

    FDA Adverse Event
    Malfunction ·DATASCOPE CORP. - MAHWAH·Product code DSP·March 17, 2023

    HEART START XL

    FDA Adverse Event
    Malfunction ·PHILIPS NORTH AMERICA LLC·Product code MKJ·August 12, 2025

    DRIVER SHAFT, T-15, SHORT

    FDA Adverse Event
    Malfunction ·ARTHREX, INC.·Product code LXH·March 18, 2025

    ASR UNI FEMORAL IMPL SIZE 47

    FDA Adverse Event
    Injury ·DEPUY INTERNATIONAL LTD - 8010379·Product code KWA·March 13, 2013

    OXFORD UNICOMPARTMENTAL KNEE PHASE 3 RIGHT MEDIAL TIBIAL TRAY STD SZ C

    FDA Adverse Event
    Injury ·BIOMET UK LTD·Product code NRA·February 25, 2011

    PULMONETIC

    FDA Adverse Event
    Malfunction ·CARDINAL HEALTH 203/PULMONETIC SYSTEMS, INC.·Product code CBK·February 25, 2008

    CARDIOSAVE HYBRID, TYPE B PLUG

    FDA Adverse Event
    Malfunction ·DATASCOPE CORP.·Product code DSP·July 31, 2025

    CARDIOSAVE HYBRID, TYPE B PLUG

    FDA Adverse Event
    Malfunction ·DATASCOPE CORP. - MAHWAH·Product code DSP·February 2, 2023

    CARDIOSAVE HYBRID, TYPE B PLUG

    FDA Adverse Event
    Malfunction ·DATASCOPE CORP.·Product code DSP·October 18, 2024

    CARDIOSAVE HYBRID, 3.1 EDITION

    FDA Adverse Event
    Malfunction ·DATASCOPE CORP.·Product code DSP·January 15, 2025