BEUDAMED
    8 results · 20ms · Sources: EU EUDAMED, US FDA

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    SKAFFOLD CIS

    FDA 510(k)
    FDA Unclassified ·Unknown

    MicroSelectron Digital

    FDA UDI
    Nucletron B.V.·08717213033238·Coupling Treatment Tube for Metal Needles (21)

    HANDHELD MANUAL BREAST PUMP (AVENT MANUAL BREAST PUMP)

    FDA 510(k)
    FDA Class 1 ·Obstetrics/Gynecology

    ENDOPATH NON-BLADED SOLID OBTURATOR TROCAR SYSTEM

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

    LCS UNI BEAR INSRT SZ3 10.0MM

    FDA Adverse Event
    Injury ·8010379 DEPUY INTL., LTD.·Product code NJL·May 14, 2013

    DYONICS

    FDA Adverse Event
    Malfunction ·SMITH & NEPHEW ENDOSCOPY·Product code HAB·May 26, 2011

    PERCLOSE PROGLIDE 6F SUTURE MEDIATED CLOSURE (SMC) SYSTEM

    FDA Adverse Event
    Injury ·ABBOTT VASCULAR REDWOOD CITY·Product code MGB·August 13, 2008

    ACCOLADE DR EL MRI (Model L331)

    FDA Enforcement
    Class I ·Ongoing·Boston Scientific Corporation·October 22, 2025