BEUDAMED
    34 results · 32ms · Sources: EU EUDAMED, US FDA

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    Sunrise SA

    Manufacturer
    🇧🇪 Belgium·2 Basic UDI-DIs·5 Devices

    SUNRISE SA

    FDA registration
    SUNRISE SA·1 product·🇧🇪 Belgium

    Sunrise sensor

    Device
    EU MDR · Eu Md Class 1 ·Sunrise SA·Not intended for eu market

    Sunrise sensor

    Device
    EU MDR · Eu Md Class 1 ·Sunrise SA·Not intended for eu market

    Sunrise sensor

    Device
    EU MDR · Eu Md Class 1 ·Sunrise SA·On the market·3 countries

    Sunrise Sleep Disorder Diagnostic Aid

    Device
    EU MDR · Eu Md Class 2a ·Sunrise SA·On the market·6 countries

    Sunrise sensor

    Device
    EU MDR · Eu Md Class 1 ·Sunrise SA·On the market·2 countries

    Sunrise Sleep Disorder Diagnostic Aid

    Basic UDI-DI
    EU MDR · Eu Md Class 2a ·Sunrise SA·1 device

    Sunrise sensor

    Basic UDI-DI
    EU MDR · Eu Md Class 1 ·Sunrise SA·4 devices

    ZIPPIE VOYAGE

    FDA Adverse Event
    Malfunction ·SUNRISE MEDICAL (US) LLC·Product code INM·December 3, 2021

    Sunrise Medical AS

    Manufacturer
    🇳🇴 Norway

    GUARDIAN

    FDA Adverse Event
    (MARS PRO)·Product code IKX·August 31, 2006

    GUARDIAN

    FDA Adverse Event
    Malfunction ·R POON·Product code INN·April 5, 2006

    GUARDIAN

    FDA Adverse Event
    Injury ·ZHONGSHAN A&E MACHINERY INDUSTRY CO., LTD.·Product code ITJ·July 7, 2006

    QUICKIE

    FDA Adverse Event
    Malfunction ·SUNRISE MEDICAL INC.·Product code IOR·December 28, 2007

    QUICKIE RHYTHM

    FDA Adverse Event
    Malfunction ·SUNRISE MEDICAL·Product code ITI·May 4, 2007

    QUICKIE QM710

    FDA Adverse Event
    Injury ·SUNRISE MEDICAL (US) LLC.·Product code ITI·July 2, 2013

    QUICKIE

    FDA Adverse Event
    Injury ·SUNRISE MEDICAL, INC.·Product code IOR·May 27, 2010

    HOYER LIFT

    FDA Adverse Event
    Other ·SUNRISE MEDICAL LTC·Product code FSA·April 12, 2005

    QUICKIE Q7

    FDA Adverse Event
    Injury ·SUNRISE MEDICAL (US) LLC·Product code IOR·January 14, 2014