BEUDAMED
    10 results · 23ms · Sources: EU EUDAMED, US FDA

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    CEDIA DIGOXIN PLUS ASSAY

    FDA 510(k)
    FDA Class 2 ·Clinical Toxicology

    De Soutter Medical

    FDA UDI
    DE SOUTTER MEDICAL LIMITED·05051471122949·K-WIRE - SINGLE TROCAR 1.6mm DIA x 200mm

    FIBRINOGEN UPTAKE SYS -VARIOUS MODELS

    FDA 510(k)
    FDA Class 1 ·Ear, Nose, Throat

    ACCU-CHEK (R) EASY (TM) BLOOD GLUCOSE SYSTEM

    FDA 510(k)
    FDA Class 2 ·Clinical Chemistry

    SYNCHRON® CK 2 X 400

    FDA Adverse Event
    Malfunction ·BECKMAN COULTER, INC.·Product code CKA·May 10, 2011

    AUTOSOFT XC

    FDA Adverse Event
    Malfunction ·UNOMEDICAL A/S·Product code FPA·August 8, 2024

    NATURALYTE

    FDA Adverse Event
    Death ·FRESENIUS MEDICAL CARE NORTH AMERICA·Product code KPO·June 27, 2014

    OPERA

    FDA Adverse Event
    Malfunction ·BHM MEDICAL INC.·Product code FSA·December 8, 2010

    9800

    FDA Adverse Event
    Malfunction ·GE OEC MEDICAL SYSTEMS (SLC)·Product code JAA·January 3, 2013

    IRC2100 W/ 210 LIGHTGUIDE

    FDA Adverse Event
    Malfunction ·COOPERSURGICAL, INC.·Product code KNS·August 28, 2019