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

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    Filters Regulation: Us FDA ×

    ANCHOR Tissue Retrieval System

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

    Epredia

    FDA UDI
    SHANDON DIAGNOSTICS LIMITED·05051663517836·CTM6 coverslipper- Accessory

    VASCOPRESS SEQUENTIAL DVT PUMP

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    MIRAGE MICRO

    FDA 510(k)
    FDA Class 2 ·Anesthesiology

    AQUILEX FLUID CONTROL SYSTEM

    FDA Adverse Event
    Malfunction ·W.O.M. WORLD OF MEDICINE GMBH·Product code HIG·March 12, 2020

    BD PRECISIONGLIDE¿ SHORT-BEVEL NEEDLE

    FDA Adverse Event
    Malfunction ·BD MEDICAL (BD WEST) MEDICAL SURGICAL·Product code FMI·April 18, 2022

    FINELINE II

    FDA Adverse Event
    Injury ·CPI - DEL CARIBE·Product code NVN·July 23, 2011

    PFC SIGMARP CV TB/IN S3 12.5

    FDA Adverse Event
    Injury ·9616671 DEPUY (IRELAND)·Product code NJL·June 17, 2013

    HIRES 90K

    FDA Adverse Event
    Malfunction ·ADVANCED BIONICS LLC·Product code MCM·September 19, 2008

    UNKNOWN

    FDA Adverse Event
    Injury ·COOK INC·Product code DYB·June 27, 2024

    MICROPUNCTURE TRANSITIONLESS ACCESS SET

    FDA Adverse Event
    Injury ·COOK INC·Product code DYB·March 29, 2022