BEUDAMED
    7 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 ×

    AMBU TUBECHECK

    FDA 510(k)
    FDA Class 2 ·Anesthesiology

    FUKUDA DENSHI DYNASCOPE MODEL DS-7000/7000M PATIENT MONITOR

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    Portable X-ray System (Model: MiniX-V, Mini X-S)

    FDA 510(k)
    FDA Class 2 ·Dental

    COULTER® LH 750 HEMATOLOGY ANALYZER

    FDA Adverse Event
    Malfunction ·BECKMAN COULTER·Product code GKZ·February 28, 2013

    ACCU-CHEK SPIRIT

    FDA Adverse Event
    Malfunction ·ROCHE INSULIN DELIVERY SYSTEM INC.·Product code LZG·January 14, 2011

    HOMECHOICE AUTOMATED PD SET WITH CASSETTE

    FDA Adverse Event
    Malfunction ·BAXTER HEALTHCARE - MOUNTAIN HOME·Product code FKX·August 5, 2014

    ARCHITECT C16000 SYSTEM

    FDA Adverse Event
    Malfunction ·ABBOTT MANUFACTURING INC·Product code JJE·May 10, 2019