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

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    MEDTRONIC SOFAMOR DANEK BIPHASIC CALCIUM PHOSPHATE (BCP) BONE VOID FILLER

    FDA 510(k)
    FDA Class 2 ·Dental

    Zirlux

    FDA UDI
    HENRY SCHEIN, INC.·H65890107011·Zirlux Guide Pin

    EsCom 100 A1 Syringe

    FDA UDI
    Spident Co., Ltd.·08809262955217·Nano-hybrid universal composite resin for poste...

    LightScalpel

    FDA UDI
    Lightscalpel, LLC·00851842007128·Accessory Tool, LS Handpieces

    JOBST Custom Seamless Soft

    FDA UDI
    BSN-Jobst GmbH·04059993124756·CUSTOM SEAMLESS SOFT 1/PANTY/CLOSED TOE/FOR MAN...

    HUMAN IGG SUBCLASS KIT USE WITH THE BECKMAN IMAGE ANALYZER

    FDA 510(k)
    FDA Class 2 ·Immunology

    LIVESURE THC SCREEN TEST

    FDA 510(k)
    FDA Class 2 ·Clinical Toxicology

    AUTOSOFT XC

    FDA Adverse Event
    Malfunction ·UNOMEDICAL DEVICES S.A. DE C.V.·Product code FPA·July 31, 2025

    AUTOSOFT XC

    FDA Adverse Event
    Malfunction ·UNOMEDICAL DEVICES S.A. DE C.V.·Product code FPA·July 31, 2025

    INSET

    FDA Adverse Event
    Malfunction ·UNOMEDICAL DEVICES S.A. DE C.V.·Product code FPA·September 23, 2025

    DAKOTA

    FDA Adverse Event
    Injury ·BOSTON SCIENTIFIC CORPORATION·Product code FFL·January 30, 2023

    HEARTWARE VENTRICULAR ASSIST SYSTEM - PUMP

    FDA Adverse Event
    Death ·HEARTWARE, INC.·Product code DSQ·October 13, 2020

    IMAGER II UROLOGY TORQUEABLE CATHETER

    FDA Adverse Event
    Injury ·BOSTON SCIENTIFIC CORPORATION·Product code KOD·April 10, 2023

    QUICK SET

    FDA Adverse Event
    Injury ·MEDTRONIC MINIMED·Product code FPA·April 9, 2026

    QUICK SET

    FDA Adverse Event
    Injury ·MEDTRONIC MINIMED·Product code FPA·April 9, 2026

    QUICK SET

    FDA Adverse Event
    Injury ·MEDTRONIC MINIMED·Product code FPA·April 9, 2026

    QUICK SET

    FDA Adverse Event
    Injury ·MEDTRONIC MINIMED·Product code FPA·April 9, 2026

    QUICK SET

    FDA Adverse Event
    Injury ·MEDTRONIC MINIMED·Product code FPA·April 9, 2026

    X-Guide Handpiece Adaptor Sleeve 1, Model P010701

    FDA Recall
    Open, Classified ·X-NAV Technologies, LLC·Product code QRY·March 4, 2024

    PINNACLE MTL INS NEUT36IDX50OD

    FDA Adverse Event
    Malfunction ·DEPUY ORTHOPAEDICS INC US·Product code KWA·March 19, 2013