BEUDAMED
    79 results · 21ms · Sources: EU EUDAMED, US FDA

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    SIGNA 7.0T

    FDA 510(k)
    FDA Class 2 ·Radiology

    EarQ

    FDA UDI
    Oticon A/S·05707131357090·G30 S, MINIRITE R LI-ION 2.4G C093 EARQ

    CODMAN

    FDA UDI
    Cerenovus, Inc.·10886704001300·CODMAN SLIM-LINE Aneurysm Clip Slightly Curved ...

    OsteoMed

    FDA UDI
    OSTEOMED LLC·00845694031356·1.5mm Drill, Quick Release

    OsteoMed

    FDA UDI
    Provision·B504OM32016150·

    3D Printed Interbody Systems

    FDA UDI
    Seaspine Orthopedics Corporation·10889981303860·2-Hole No-Profile Interbody, 31mm x 24mm x 16mm...

    Meridian

    FDA UDI
    Seaspine Orthopedics Corporation·10889981215286·No-Profile Interbody, 31mm x 24mm x 16mm, 15 Deg

    Meridian

    FDA UDI
    Seaspine Orthopedics Corporation·10889981309749·Trial Rasp, 31mm x 24mm x 16mm, 15 Deg

    ABSORBENT PAPER POINTS

    FDA UDI
    DiaDent Group International·08806383554534·"An absorbent paper points is an endodontic pap...

    ABSORBENT PAPER POINTS

    FDA UDI
    DiaDent Group International·08806383512497·"An absorbent paper points is an endodontic pap...

    NA

    FDA UDI
    aap Implantate AG·04042409049378·K-wire with 2 trocar points, ø1.6, L 150

    HUNTER SCIENTIFIC INJECTION PIPETTES

    FDA 510(k)
    FDA Class 2 ·Obstetrics/Gynecology

    BAXTER ACCURA SYSTEM, MODEL 5M5660

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

    RV LEAD

    FDA Adverse Event
    Malfunction ·UNKNOWN·Product code NVY·August 12, 2023

    OsteoMed

    FDA UDI
    OSTEOMED LLC·00845694073301·HPS 1.5mm Drill, Quick Release Sterile Qty 2

    NA

    FDA UDI
    aap Implantate AG·04042409117442·K-wire with 2 trocar points, ø1.6, L 150

    IMPLANTABLE CARDIOVERTER DEFIBRILLATOR (NON-CRT)

    FDA Adverse Event
    Malfunction ·ABBOTT MEDICAL / ST. JUDE·Product code LWS·May 28, 2024

    ANIMAS VIBE

    FDA Adverse Event
    Malfunction ·ANIMAS CORPORATION·Product code LZG·January 21, 2016

    VICRYL POLYGLACTIN 910 SUTURE UNKNOWN PRODUCT

    FDA Adverse Event
    Injury ·ETHICON INC.·Product code GAM·July 11, 2018

    THERMACARE LOWER BACK & HIP

    FDA Adverse Event
    Injury ·PFIZER CONSUMER HEALTH CARE·Product code IMD·October 17, 2016