BEUDAMED
    708 results · 22ms · Sources: EU EUDAMED, US FDA

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    IVOLVE NASAL MASK, IVOLVE FULL FACE MASK, IVOLVE N2

    FDA 510(k)
    FDA Class 2 ·Anesthesiology

    Tasso+ Convenience Kit

    FDA UDI
    Tasso Inc.·00850038691011·

    Medke

    FDA UDI
    Shenzhen MedKe Technology Co., Ltd·06971018115250·

    Portex

    FDA UDI
    ICU MEDICAL, INC.·15019517084764·

    ADVIA Centaur® Sample Tips

    FDA UDI
    Siemens Healthcare Diagnostics Inc.·00630414222608·Pipette tip

    PROVEN REVISION FEMORAL AND PROVEN REVISION TIBIAL INSERT

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    IPL THERAPY SYSTEM

    FDA 510(k)
    FDA Class 2 ·General, Plastic Surgery

    COULTER® LH 500 HEMATOLOGY INSTRUMENT

    FDA Adverse Event
    Malfunction ·BECKMAN COULTER·Product code GKZ·May 29, 2013

    ENRHYTHM DR

    FDA Adverse Event
    Injury ·MEDTRONIC MED REL, INC.·Product code DXY·June 16, 2011

    POWERLINK SYSTEM

    FDA Adverse Event
    Injury ·ENDOLOGIX, INC.·Product code MIH·August 20, 2008

    PENTAX

    FDA Adverse Event
    Malfunction ·HOYA CORPORATION PENTAX TOKYO OFFICE·Product code FDS·July 30, 2021

    PENTAX

    FDA Adverse Event
    Malfunction ·HOYA CORPORATION PENTAX TOKYO OFFICE·Product code FDS·July 21, 2021

    PENTAX

    FDA Adverse Event
    Malfunction ·HOYA CORPORATION PENTAX TOKYO OFFICE·Product code FDS·July 24, 2021

    PENTAX

    FDA Adverse Event
    Malfunction ·HOYA CORPORATION PENTAX TOKYO OFFICE·Product code FDS·July 24, 2021

    PENTAX

    FDA Adverse Event
    Malfunction ·HOYA CORPORATION PENTAX TOKYO OFFICE·Product code FDS·September 10, 2021

    PENTAX

    FDA Adverse Event
    Malfunction ·HOYA CORPORATION PENTAX TOKYO OFFICE·Product code FDS·December 26, 2022

    PENTAX

    FDA Adverse Event
    Malfunction ·HOYA CORPORATION PENTAX TOKYO OFFICE·Product code FDS·September 22, 2022

    PENTAX

    FDA Adverse Event
    Malfunction ·HOYA CORPORATION PENTAX TOKYO OFFICE·Product code FDS·February 7, 2022

    PENTAX

    FDA Adverse Event
    Malfunction ·HOYA CORPORATION PENTAX TOKYO OFFICE·Product code FDS·March 1, 2022

    PENTAX

    FDA Adverse Event
    Malfunction ·HOYA CORPORATION PENTAX TOKYO OFFICE·Product code FDS·February 3, 2022