BEUDAMED
    10 results · 27ms · Sources: EU EUDAMED, US FDA

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    ACUCISE GUIDEWIRE EXCHANGE SHEATH

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

    PowerPumpTM dp System

    FDA UDI
    INSIGHTRA MEDICAL, INC.·17350021986105·

    Ophthalmic Scissors

    FDA UDI
    KATENA PRODUCTS, INC.·00841668105061·CASTROVIEJO CORNEOSCLERAL SCISSORS SM LT

    Gen. Acces/ Instr. Tip Guard

    FDA UDI
    KATENA PRODUCTS, INC.·00841668112250·SURG-I-BAND YELLOW

    M9 DIAGNOSTIC ULTRASOUND SYSTEM, M9T DIAGNOSTIC ULTRASOUND SYSTEM, M9CV DIAGNOSTIC ULTRASOUND SYSTEM

    FDA 510(k)
    FDA Class 2 ·Radiology

    REMSTAR AUTO WITH C-FLEX CPAP SYSTEM

    FDA 510(k)
    FDA Class 2 ·Anesthesiology

    REMSTAR AUTO M SERIES

    FDA Adverse Event
    Injury ·RESPIRONICS, INC.·Product code BZD·April 14, 2024

    WAVELIGHT EX500 EXCIMER LASER

    FDA Adverse Event
    Injury ·WAVELIGHT GMBH·Product code LZS·June 30, 2014

    PERCLOSE PROGLIDE 6F SUTURE MEDIATED CLOSURE (SMC) SYSTEM

    FDA Adverse Event
    Injury ·AV-TEMECULA-CT·Product code MGB·February 4, 2013

    ALL POLY CONSTRAINED INSERT 50MM

    FDA Adverse Event
    Malfunction ·STRYKER ORTHOPAEDICS MAHWAH·Product code KWZ·December 7, 2010