BEUDAMED
    44 results · 23ms · Sources: EU EUDAMED, US FDA

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    CARDIAC SCANNER AND PROCESSING SYSTEM

    FDA 510(k)
    FDA Class 2 ·Radiology

    Humelock II Cemented Shoulder System

    FDA UDI
    FX SOLUTIONS·03701037302958·HUMELOCK II LONG STEM TA6V SIZE 07 LG200 mm CEM...

    NA

    FDA UDI
    Stryker Leibinger GmbH & Co. KG·04546540490582·MINI PLATE, STRAIGHT, WITH BAR

    TALOS®-C HA

    FDA UDI
    MEDITECH SPINE, LLC·B167521105070·

    NIDO Pedicle Screw System

    FDA UDI
    Kalitec Direct LLC·B07315K1100070·Tray Insert 1, NIDO

    LAT ASSEMBLY, RAD STEM IMPLANT,COLLAR 6MM,SIZE2

    FDA Adverse Event
    Malfunction ·STRYKER GMBH·Product code KWI·August 29, 2017

    UNKNOWN COLLAR R HEAD LATERAL STEM

    FDA Adverse Event
    Malfunction ·STRYKER GMBH·Product code LXH·August 29, 2017

    VISTAKON (METHAFILCON A) CONTACT LENSES

    FDA 510(k)
    FDA Class 2 ·Ophthalmic

    XRES BLOOD COLLECTION RESERVOIR

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    MEGA SUTURECUT

    FDA Adverse Event
    Malfunction ·INTUITIVE SURGICAL, INC·Product code NAY·May 8, 2013

    PARADIGM REAL-TIME REVEL INSULIN INFUSION PUMP

    FDA Adverse Event
    Malfunction ·MEDTRONIC MINIMED·Product code OYC·September 23, 2014

    COLLEAGUE PRE P1.7

    FDA Adverse Event
    Malfunction ·BAXTER HEALTHCARE - SINGAPORE·Product code FRN·June 1, 2011

    SPECIFIC DEVICE NOT REPORTED

    FDA Adverse Event
    Injury ·EXACTECH, INC.·Product code JWH·October 22, 2024

    LOGIC TIBIA IMPLANT PSC INSERT, SZ 5, 13MM

    FDA Adverse Event
    Injury ·EXACTECH, INC.·Product code JWH·April 13, 2023

    SPECIFIC DEVICE NOT REPORTED

    FDA Adverse Event
    Injury ·EXACTECH, INC.·Product code JWH·December 17, 2024

    LOGIC FEMORAL PS CEM LEFT SZ 3.5

    FDA Adverse Event
    Injury ·EXACTECH, INC.·Product code JWH·March 5, 2025

    LOGIC TIBIA IMPLANT PSC INSERT, SZ 4, 9MM

    FDA Adverse Event
    Injury ·EXACTECH, INC.·Product code JWH·June 30, 2022

    LOGIC TIBIA IMPLANT PSC INSERT, SZ 3.5, 11MM

    FDA Adverse Event
    Injury ·EXACTECH, INC.·Product code JWH·September 5, 2024

    LOGIC TIBIA IMPLANT PSC INSERT, SZ 1, 13MM

    FDA Adverse Event
    Injury ·EXACTECH, INC.·Product code JWH·September 11, 2024

    SPECIFIC DEVICE NOT REPORTED

    FDA Adverse Event
    Injury ·EXACTECH, INC.·Product code JWH·October 22, 2024