BEUDAMED
    52 results · 21ms · Sources: EU EUDAMED, US FDA

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    MODIFICATION TO JMS APHERESIS NEEDLE

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

    PowerPICC Provena

    FDA UDI
    Bard Access Systems, Inc.·00801741154683·Catheter Placement Kit

    CUSTOM PROCEDURE KIT

    FDA UDI
    MEDIVATORS INC.·40677964006942·CUSTOM PROCEDURE KIT

    Bard Stoma Measuring Device

    FDA UDI
    Bard Access Systems, Inc.·00801741086847·Bard Stoma Measuring Device 28F

    AtriCure System Cart

    FDA UDI
    ATRICURE, INC.·10840143904035·CRYO CART KIT ASSEMBLY - TWO TANK SUPPORTS

    AtriCure System Cart

    FDA UDI
    ATRICURE, INC.·00818354011920·CRYO CART KIT ASSEMBLY - TWO TANK SUPPORTS

    LIFENET ASSET EXPORT 32-BIT

    FDA UDI
    PHYSIO-CONTROL, INC.·00883873862902·LIFENET ASSET EXPORT 32-BIT 5.4.1.2

    TUFF IMPLANT

    FDA Adverse Event
    Malfunction ·NORIS MEDICAL LTD·Product code DZE·July 14, 2024

    MIDAS TOUCH NITRILE EXAMINATION GLOVES-POWDERED

    FDA 510(k)
    FDA Class 1 ·General Hospital

    DRG AURICA ELISA TESTOSTERONE KIT

    FDA 510(k)
    FDA Class 1 ·Clinical Chemistry

    TUFF IMPLANT

    FDA Adverse Event
    Injury ·NORIS MEDICAL LTD·Product code DZE·May 13, 2024

    TUFF IMPLANT

    FDA Adverse Event
    Injury ·NORIS MEDICAL LTD·Product code DZE·May 13, 2024

    TUFF IMPLANT

    FDA Adverse Event
    Injury ·NORIS MEDICAL LTD·Product code DZE·August 15, 2024

    TAXUS EXPRESS2 PACLITAXEL-ELUTING CORONARY STENT SYSTEM

    FDA Adverse Event
    Injury ·BOSTON SCIENTIFIC CORP.·Product code NIO·April 30, 2007

    TUFF IMPLANT

    FDA Adverse Event
    Injury ·NORIS MEDICAL LTD·Product code DZE·July 10, 2024

    TUFF IMPLANT

    FDA Adverse Event
    Injury ·NORIS MEDICAL LTD·Product code DZE·February 24, 2026

    OT VERIO IQ METER

    FDA Adverse Event
    Malfunction ·LIFESCAN EUROPE, A DIVISION OF CILAG GMBH INTL·Product code NBW·March 13, 2013

    EON RECHARGEABLE IPG, 16-CHANNEL

    FDA Adverse Event
    Injury ·ST. JUDE MEDICAL - NEUROMODULATION DIVISION·Product code LGW·February 17, 2011

    LIFESHIELD FILTER SOLUSET

    FDA Adverse Event
    Malfunction ·HOSPIRA DE COSTA RICA LTD.·Product code FPB·February 18, 2008

    TUFF IMPLANT

    FDA Adverse Event
    Injury ·NORIS MEDICAL LTD·Product code DZE·May 2, 2024