BEUDAMED
    9 results · 34ms · Sources: EU EUDAMED, US FDA

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    CRANK FRAME RETRACTOR

    FDA 510(k)
    FDA Class 2 ·Neurology

    Multi-Sideport Catheter Infusion Set

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    ADPHARMA OCCLUDE AND OCCLUDE F DENTIN TUBULE AGENT

    FDA 510(k)
    FDA Class 2 ·Dental

    EDWARDS SAPIEN TRANSCATHETER HEART VALVE

    FDA Adverse Event
    Injury ·EDWARDS LIFESCIENCES·Product code NPT·June 18, 2014

    SELEX/M2A MAGNUM MODULAR HEAD 40MM HEAD DIAMETER

    FDA Adverse Event
    Injury ·BIOMET ORTHOPEDICS·Product code KWA·October 25, 2010

    SYNCHROMED II

    FDA Adverse Event
    Injury ·MDT PUERTO RICO OPERATIONS CO·Product code LKK·December 20, 2012

    MULTI-SIDEPORT DUAL CHECK VALVE CATHETER INFUSION SET

    FDA Adverse Event
    Injury ·COOK INC·Product code KRA·April 27, 2022

    MULTI-SIDEPORT DUAL CHECK VALVE CATHETER INFUSION SET

    FDA Adverse Event
    Malfunction ·COOK INC·Product code KRA·April 11, 2022

    MULTI-SIDEPORT DUAL CHECK VALVE CATHETER INFUSION SET

    FDA Adverse Event
    Malfunction ·COOK INC·Product code KRA·August 19, 2022