BEUDAMED
    12 results · 28ms · Sources: EU EUDAMED, US FDA

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    CEZANNE II INTERBODY FUSION SYSTEM

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    K131982

    FDA Adverse Event
    Malfunction ·RESPIRONICS, INC.·Product code BZD·February 23, 2024

    2.4 SMARTNAIL, MODELS 532416, 532425, 532435, 532445

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    OPTETRAK LOGIC COMBINATION TIBIAL TRAY

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    OT VERIO TEST STRIPS

    FDA Adverse Event
    Malfunction ·LIFESCAN EUROPE, A DIVISION OF CILAG GMBH INTL·Product code NBW·May 29, 2013

    PARADIGM REAL-TIME REVEL INSULIN INFUSION PUMP

    FDA Adverse Event
    Malfunction ·MEDTRONIC MINIMED·Product code OYC·October 1, 2014

    INTERSTIM II

    FDA Adverse Event
    Injury ·MEDTRONIC PUERTO RICO OPERATIONS CO.·Product code EZW·October 7, 2015

    NCB®, PERIPROSTHETIC FEMUR PLATE, DISTAL, RIGHT, 15 HOLES, 317 MM

    FDA Adverse Event
    Injury ·ZIMMER GMBH·Product code HRS·June 6, 2024

    LGC TIBIAL FIT TRAY CEM SZ 3.5F / 3.5T

    FDA Adverse Event
    Injury ·EXACTECH, INC.·Product code JWH·January 6, 2025

    SMARTNAIL

    FDA Adverse Event
    Injury ·CONMED CORPORATION·Product code MAI·July 29, 2019

    LOGIC FEMORAL PS CEM RIGHT SZ 2

    FDA Adverse Event
    Injury ·EXACTECH, INC.·Product code JWH·September 4, 2024

    OPTETRAK HI-FLEX TIBIAL INSERT SZ 4 11MM

    FDA Adverse Event
    Injury ·EXACTECH, INC.·Product code JWH·August 25, 2022