BEUDAMED
    6 results · 18ms · 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.

    ALANINE AMINOTRANSFERASE TEST ITEM NO. 65652

    FDA 510(k)
    FDA Class 1 ·Clinical Chemistry

    FILTRARE TM ALLVENT TM

    FDA 510(k)
    FDA Class 2 ·General Hospital

    MODEL 78210A TELEMETRY TRANSMITTER

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    SILIC FOLEY CATH 5/10ML/5

    FDA Adverse Event
    Malfunction ·COLOPLAST A/S·Product code EZL·June 19, 2014

    UNICEL® DXC 600I SYNCHRON® ACCESS® CLINICAL SYSTEM (CRATED)

    FDA Adverse Event
    Malfunction ·BECKMAN COULTER INC.·Product code MMI·October 27, 2010

    OT VERIO PRO METER

    FDA Adverse Event
    Malfunction ·LIFESCAN EUROPE, A DIVISION OF CILAG GMBH INTL·Product code NBW·December 22, 2012