BEUDAMED
    19 results · 63ms · Sources: EU EUDAMED, US FDA

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    Pulse Scientific Inc.

    FDA UDI
    Pulse Scientific Inc·00628055726036·

    Pulse Scientific Inc.

    FDA UDI
    Pulse Scientific Inc·00628055726005·

    Pulse Scientific Inc.

    FDA UDI
    Pulse Scientific Inc·00628055726029·

    Pulse Scientific Inc.

    FDA UDI
    Pulse Scientific Inc·00628055726012·

    FARAWAVE PULSED FIELD ABLATION CATHETER

    FDA Adverse Event
    Injury ·BOSTON SCIENTIFIC CORPORATION·Product code QZI·September 30, 2025

    EZ STEER NAV

    FDA Adverse Event
    Injury ·BIOSENSE WEBSTER INC·Product code LPB·May 8, 2026

    INTELLANAV STABLEPOINT OPEN-IRRIGATED

    FDA Adverse Event
    Injury ·BOSTON SCIENTIFIC CORPORATION·Product code OAE·May 13, 2026

    FARADRIVE STEERABLE SHEATH

    FDA Adverse Event
    Injury ·BOSTON SCIENTIFIC CORPORATION·Product code DRA·May 13, 2026

    AUTOLITH TCH 1.9FR PROBE, 375CM DS BSC

    FDA Adverse Event
    Injury ·NORTHGATE TECHNOLOGIES INC.·Product code FFK·March 12, 2026

    VERCISE GENUS?

    FDA Adverse Event
    Injury ·BOSTON SCIENTIFIC NEUROMODULATION CORPORATION·Product code NHL·June 3, 2025

    THERMOCOOL® SMART TOUCH® SF BI-DIRECTIONAL NAVIGATION CATHETER

    FDA Adverse Event
    Injury ·BIOSENSE WEBSTER INC·Product code LPB·April 11, 2024

    SHOCKWAVE C2 CORONARY INTRAVASCULAR LITHOTRIPSY (IVL) CATHETER

    FDA Adverse Event
    Injury ·SHOCKWAVE MEDICAL, INC.·Product code QMG·July 23, 2025

    NA

    FDA Adverse Event
    Injury ·STERILMED, INC.·Product code OWQ·November 21, 2024

    TACTICATH¿ CONTACT FORCE ABLATION CATHETER, SENSOR ENABLED¿

    FDA Adverse Event
    Injury ·ST. JUDE MEDICAL·Product code OAE·January 31, 2024

    PULSE GEN MODEL UNKOWN

    FDA Adverse Event
    Injury ·CYBERONICS - HOUSTON·Product code MUZ·July 28, 2024

    PULSE GENERATOR MODEL UNKNOWN

    FDA Adverse Event
    Malfunction ·LIVANOVA USA, INC.·Product code MUZ·July 28, 2024

    AUTOLITH TOUCH

    FDA Adverse Event
    Malfunction ·NORTHGATE TECHNOLOGIES INC.·Product code FFK·February 5, 2020

    SHOCKWAVE IVL SYSTEM WITH THE SHOCKWAVE M5+ PERIPHERAL IVL CATHETER

    FDA Adverse Event
    Malfunction ·SHOCKWAVE MEDICAL, INC.·Product code PPN·January 2, 2026

    FLEXIVA (TM) HIGH POWER SINGLE-USE LASER FIBER

    FDA Adverse Event
    Malfunction ·BOSTON SCIENTIFIC - MARLBOROUGH·Product code GEX·May 13, 2015