BEUDAMED
    14 results · 25ms · Sources: EU EUDAMED, US FDA

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    Filters Regulation: Us FDA ×

    Mortara Surveyor Patient Monitor

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    PRECISION PRESS TACK / INTRADERM, SEVEN STAR AND ACUPUNCTURE NEEDLES; ALPHA AND FINE POINT ACUPUNCTURE NEEDLES

    FDA 510(k)
    FDA Class 2 ·General Hospital

    SEDECAL MOBILE DIGITAL DIAGNOSTIC X-RAY

    FDA 510(k)
    FDA Class 2 ·Radiology

    ENDOTAK RELIANCE

    FDA Adverse Event
    Injury ·CPI - DEL CARIBE·Product code NVY·July 14, 2011

    CHARGING SYSTEM

    FDA Adverse Event
    Injury ·ST. JUDE MEDICAL - NEUROMODULATION·Product code LGW·June 5, 2013

    XPERT SELF-EXPANDING TRANSHEPATIC BILIARY STENT SYSTEM

    FDA Adverse Event
    Malfunction ·ABBOTT VASCULAR SWITZERLAND·Product code FGE·September 15, 2008

    UNKNOWN JOINT REPAIR DEVICE

    FDA Adverse Event
    Injury ·SMITH & NEPHEW, INC.·Product code MBI·January 6, 2026

    UNKN JOINT REPAIR DEV

    FDA Adverse Event
    Injury ·SMITH & NEPHEW, INC.·Product code MBI·January 6, 2026

    UNKNOWN

    FDA Adverse Event
    Injury ·SMITH & NEPHEW, INC.·Product code MBI·January 6, 2026

    ATTACHMENT BIT

    FDA Adverse Event
    Malfunction ·RTI SURGICAL·Product code LXH·February 4, 2021

    UNKNOWN JOINT REPAIR DEV

    FDA Adverse Event
    Injury ·SMITH & NEPHEW, INC.·Product code MBI·January 6, 2026

    UNKNOWN JOINT REPAIR DEVICE

    FDA Adverse Event
    Injury ·SMITH & NEPHEW, INC.·Product code MBI·January 6, 2026

    UNKN JOINT REPAIR DEV

    FDA Adverse Event
    Injury ·SMITH & NEPHEW, INC.·Product code MBI·January 6, 2026

    UNKN JOINT REPAIR DEV

    FDA Adverse Event
    Injury ·SMITH & NEPHEW, INC.·Product code MBI·January 6, 2026