BEUDAMED
    12 results · 31ms · Sources: EU EUDAMED, US FDA

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    SMITH & NEPHEW ULTRATAPE

    FDA 510(k)
    FDA Class 2 ·General, Plastic Surgery

    HHM

    FDA UDI
    Oticon A/S·05707131258151·H160, RITE 312 WL SGR HHM

    Ophthalmic Spatula

    FDA UDI
    KATENA PRODUCTS, INC.·00841668102589·AKAHOSHI NUCLEUS SUSTAINER

    LINEAR ST

    FDA Adverse Event
    Injury ·BOSTON SCIENTIFIC NEUROMODULATION·Product code LGW·July 11, 2019

    NOVUS TTX LASER AND DELIVERY DEVICES WITH ACCESSORIES

    FDA 510(k)
    FDA Class 2 ·General, Plastic Surgery

    VESSEL GUARDIAN

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

    DEXCOM G7 CONTINUOUS GLUCOSE MONITORING SYSTEM

    FDA Adverse Event
    Malfunction ·DEXCOM, INC.·Product code QBJ·May 29, 2025

    GENISTRONG

    FDA Adverse Event
    Malfunction ·GENICON·Product code GCJ·October 15, 2017

    PUMP MMT-1715KM 630G 3ML BLACK MEDI  

    FDA Adverse Event
    Injury ·MEDTRONIC PUERTO RICO OPERATIONS CO.·Product code OZO·September 24, 2018

    ENDOTAK ENDURANCE

    FDA Adverse Event
    Injury ·CPI - DEL CARIBE·Product code LWS·October 1, 2014

    ASR ACETABULAR CUPS 58

    FDA Adverse Event
    Injury ·DEPUY INTERNATIONAL·Product code KWA·May 29, 2013

    CORE UNIVERSAL DRIVER

    FDA Adverse Event
    Malfunction ·STRYKER INSTRUMENTS KALAMAZOO·Product code HBE·June 13, 2011