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

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    Cascadia Interbody System

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    MSI Precision Specialty Instruments

    FDA UDI
    Med Saver, Inc.·00194613017859·K-Wire, Double Ended, Trocar Point, Diameter 0....

    MSI Precision Specialty Instruments

    FDA UDI
    Med Saver, Inc.·00194613017842·K-Wire, Double Ended, Trocar Point, Diameter Si...

    OsteoMed

    FDA UDI
    OSTEOMED LLC·00842528126417·Ø2.7mm Drill/Cntrsnk Cmbo Shrt, Quick Release

    ACCESS BREAST COIL 4/SMS

    FDA 510(k)
    FDA Class 2 ·Radiology

    ELITECH CLINICAL SYSTEMS HBA1C REAGENT, ELITECH CLINCAL SYSTEM HBA1C CALIBRATOR SET, ELITECH CLINICAL

    FDA 510(k)
    FDA Class 2 ·Hematology

    CHLORAPREP ONE STEP

    FDA Adverse Event
    Injury ·CAREFUSION 213, LLC 0113·Product code KXF·April 6, 2021

    CHLORAPREP ONE STEP

    FDA Adverse Event
    Injury ·CAREFUSION 213, LLC 0113·Product code KXF·April 5, 2021

    CONSULTA CRT-D

    FDA Adverse Event
    Injury ·MEDTRONIC MED REL MEDTRONIC PUERTO RICO·Product code NIK·June 10, 2013

    COLLEAGUE PRE P1.7

    FDA Adverse Event
    Malfunction ·BAXTER HEALTHCARE - SINGAPORE·Product code FRN·July 13, 2011

    LOCKING SCREW, FULLY THREADED 5X40MM

    FDA Adverse Event
    Malfunction ·STRYKER OSTEOSYNTHESIS KIEL·Product code HWC·September 10, 2008

    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

    SPECIFIC DEVICE NOT REPORTED

    FDA Adverse Event
    Injury ·EXACTECH, INC.·Product code JWH·October 26, 2023