BEUDAMED
    6 results · 23ms · 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.

    INDI KWIK (TM) CO/TWO KIT

    FDA 510(k)
    FDA Class 1 ·Microbiology

    FLOOR TO WALL OR FLOOR TO CEILING TUBESTAND;RADIOG

    FDA 510(k)
    FDA Class 1 ·Radiology

    MEDIPART LUNG AEROSOL KIT MP-1012A

    FDA 510(k)
    FDA Class 2 ·Radiology

    HOMECHOICE AUTOMATED PD SET WITH CASSETTE

    FDA Adverse Event
    Malfunction ·BAXTER HEALTHCARE - MOUNTAIN HOME·Product code FKX·June 9, 2014

    CAPSUREFIX NOVUS

    FDA Adverse Event
    Injury ·MEDTRONIC PUERTO RICO, INC.·Product code DTB·October 6, 2010

    V200 VENTILATOR

    FDA Adverse Event
    Malfunction ·RESPIRONICS CALIFORNIA, INC.·Product code CBK·December 3, 2012