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

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    Filters Regulation: Us FDA ×

    NB 1 SA Implant System

    FDA 510(k)
    FDA Class 2 ·Dental

    POWDER FREE NITRILE EXAMINATION GLOVE-BLUE (CHEMOTHERAPY)

    FDA 510(k)
    FDA Class 1 ·General Hospital

    KYPHON VuE Bone Cement

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    OT VERIO IQ METER

    FDA Adverse Event
    Malfunction ·LIFESCAN EUROPE GMBH·Product code NBW·January 8, 2019

    PLUS SL

    FDA Adverse Event
    Injury ·SMITH & NEPHEW ORTHOPEDICS AG·Product code KWY·November 5, 2008

    RX ERCP CANNULA

    FDA Adverse Event
    Malfunction ·BOSTON SCIENTIFIC - SPENCER·Product code GCJ·August 24, 2011

    4000CMS

    FDA Adverse Event
    Malfunction ·MOOG DEVICE GROUP·Product code FRN·July 2, 2013

    CRITICOOL

    FDA Adverse Event
    Malfunction ·BELMONT MEDICAL TECHNOLOGIES·Product code DWJ·January 6, 2023

    CRITICOOL

    FDA Adverse Event
    Malfunction ·BELMONT MEDICAL TECHNOLOGIES·Product code DWJ·January 8, 2023

    CRITICOOL

    FDA Adverse Event
    Malfunction ·BELMONT MEDICAL TECHNOLOGIES·Product code DWJ·December 1, 2022