BEUDAMED
    10 results · 19ms · Sources: EU EUDAMED, US FDA

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    QIAstat-Dx Respiratory Panel Mini

    FDA 510(k)
    FDA Class 2 ·Microbiology

    LEONE SPA

    FDA UDI
    LEONE SPA·08033707041061·DB BRACKETS 22 T-2 A+13 CUS U/L

    HS III PROXIMAL SEAL SYSTEM 3.8MM

    FDA Adverse Event
    Malfunction ·MAQUET CARDIOVASCULAR, LLC·Product code DXC·October 1, 2013

    THERAPY ABLATION CATHETER

    FDA Adverse Event
    Malfunction ·IRVINE BIOMEDICAL, A ST. JUDE MEDICAL COMPANY·Product code OAD·June 25, 2010

    First Sign Drug of Abuse Dip Card Test/First Sign Drug of Abuse Cup Test

    FDA 510(k)
    FDA Class 2 ·Clinical Toxicology

    AXIS I (1MP), II (2MP), III (3MP), AND V (5MP) MONOCHROME DISPLAYS

    FDA 510(k)
    FDA Class 2 ·Radiology

    HS III PROXIMAL SEAL

    FDA Adverse Event
    Malfunction ·MAQUET CARDIOVASCULAR·Product code DXC·October 1, 2013

    PORTABLE OXYGEN GENERATOR (CONCENTRATOR, HOMEFILL)

    FDA Adverse Event
    Malfunction ·INVACARE FLORIDA OPERATIONS·Product code CAW·November 11, 2014

    COLLEAGUE

    FDA Adverse Event
    Malfunction ·BAXTER HEALTHCARE - SINGAPORE·Product code FRN·September 10, 2011

    ACCU-CHEK ® SPIRIT COMBO

    FDA Adverse Event
    Malfunction ·ROCHE HEALTH SOLUTIONS, INC.·Product code LZG·July 23, 2013