BEUDAMED
    11 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 ×

    PHILIPS INTEGRIS V5000 AND BV5000

    FDA 510(k)
    FDA Class 2 ·Radiology

    XKNIFE-3

    FDA 510(k)
    FDA Class 2 ·Radiology

    TSA 5% SHEEP BLOOD (SB)/MACCONKEY AGAR #Z3033

    FDA 510(k)
    FDA Class 1 ·Microbiology

    BD FACSCALIBUR¿ FLOW CYTOMETER

    FDA Adverse Event
    Malfunction ·BECTON, DICKINSON AND COMPANY, BD BIOSCIENCES·Product code GKZ·January 31, 2023

    UNKNOWN

    FDA Adverse Event
    Injury ·UNKNOWN·Product code OTO·February 15, 2013

    FLANGE FIXTURE AND ABUTMENT

    FDA Adverse Event
    Injury ·COCHLEAR BONE ANCHORED SOLUTIONS AB·Product code LXB·August 1, 2014

    TOTAL ASR FEM IMP SZ 47

    FDA Adverse Event
    Malfunction ·DEPUY INTERNATIONAL LTD. 8010379·Product code KWA·January 12, 2011

    BD FACSCALIBUR FLOW CYTOMETER

    FDA Adverse Event
    Malfunction ·BECTON, DICKINSON AND COMPANY, BD BIOSCIENCES·Product code GKZ·March 31, 2023

    BD FACSCALIBUR¿ FLOW CYTOMETER

    FDA Adverse Event
    Malfunction ·BECTON, DICKINSON AND COMPANY, BD BIOSCIENCES·Product code GKZ·March 31, 2023

    BD FACSCALIBUR¿ FLOW CYTOMETER

    FDA Adverse Event
    Malfunction ·BECTON, DICKINSON AND COMPANY, BD BIOSCIENCES·Product code GKZ·January 20, 2023

    BD FACSCALIBUR¿ FLOW CYTOMETER

    FDA Adverse Event
    Malfunction ·BECTON, DICKINSON AND COMPANY, BD BIOSCIENCES·Product code GKZ·July 24, 2023