BEUDAMED
    6 results · 19ms · 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 ×

    PneumoLiner

    FDA 510(k)
    FDA Class 2 ·Obstetrics/Gynecology

    CONMED LINVATEC PRESTO PRELOADED WITH ONE OR TWO #2 HI-FI SUTURES

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    BELLOTA SONOHYSTEROGRAPHY CATHETER WITH CERVICAL CONE, BELLOTA SONOHYSTEROGRAPHY CATHETER WITHOUT CERVICAL CONE

    FDA 510(k)
    FDA Class 2 ·Obstetrics/Gynecology

    840 VENTILATOR

    FDA Adverse Event
    Injury ·COVIDIEN, FORMERLY NELLCOR·Product code CBK·June 25, 2013

    PENUMBRA SYSTEM SEPARATOR 032

    FDA Adverse Event
    Malfunction ·PENUMBRA, INC.·Product code NRY·July 25, 2011

    PARADIGM REAL-TIME INSULIN INFUSION PUMP

    FDA Adverse Event
    Malfunction ·MEDTRONIC PUERTO RICO OPERATIONS CO.·Product code OYC·October 22, 2014