BEUDAMED
    8 results · 20ms · 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.
    Filters Regulation: Us FDA ×

    InPen System App (MMT-8060 (iOS), MMT-8061 (Android))

    FDA 510(k)
    FDA Class 2 ·Anesthesiology

    Neuwater TM (HydrocynTM aqua)

    FDA 510(k)
    FDA Unclassified ·Unknown

    INQUIRY AFOCUS, INQUIRY AFOCUS II AND INQUIRY OPTIMA STEERABLE ELECTROPHYSIOLOGY CATHETER

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    IMP TM 4.1MM MTX FULL,10M

    FDA Adverse Event
    Injury ·ZIMMER DENTAL·Product code DZE·March 11, 2024

    BD Q-SYTE¿ LUER ACCESS SPLIT-SEPTUM STAND-ALONE DEVICE

    FDA Adverse Event
    Malfunction ·BD INFUSION THERAPY SYSTEMS INC. S.A. DE C.V.·Product code FPA·September 4, 2019

    PARADIGM REAL-TIME REVEL INSULIN INFUSION PUMP

    FDA Adverse Event
    Malfunction ·MEDTRONIC PUERTO RICO OPERATIONS CO.·Product code OYC·November 11, 2014

    RIATA PASSIVE FIXATION

    FDA Adverse Event
    Injury ·ST JUDE MEDICAL CARDIAC RHYTHM MANAGEMENT DIVISION·Product code NVY·September 10, 2011

    PHOENIX

    FDA Adverse Event
    Injury ·GAMBRO DASCO S.P.A·Product code KDI·July 23, 2013