BEUDAMED
    9 results · 18ms · Sources: EU EUDAMED, US FDA

    Get notified when this changes

    We'll email you when new records match this search — new devices, new clearances, certificate changes, or withdrawals.

    TROPONIN I ASSAY FOR THE BAYER IMMUNO 1 SYSTEM

    FDA 510(k)
    FDA Class 2 ·Clinical Chemistry

    OMNISPAN MENISCAL REPAIR 27DEG

    FDA Adverse Event
    Malfunction ·DEPUY MITEK LLC US·Product code MAI·June 25, 2020

    DIP Arthrodesis System

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    FAS-CLEAN ELECTROSURGICAL COATED ACTIVE BLADE

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

    CAPIOX HEMOCONCENTRATOR

    FDA Adverse Event
    Malfunction ·TERUMO CORPORATION, ASHITAKA·Product code KDI·March 3, 2016

    PHILIPS INFORMATION CENTER

    FDA Adverse Event
    Death ·PHILIPS MEDICAL SYSTEMS·Product code MHX·February 11, 2013

    9800

    FDA Adverse Event
    Malfunction ·GE OEC MEDICAL SYSTEMS (SLC)·Product code JAA·January 19, 2011

    ARTICULEZE M HEAD 36MM +8.5

    FDA Adverse Event
    Injury ·DEPUY ORTHOPAEDICS, INC. 1818910·Product code JDI·August 1, 2014

    OMNISPAN MENISCAL REPAIR 27DEG

    FDA Adverse Event
    Malfunction ·DEPUY MITEK LLC US·Product code MAI·May 20, 2021