BEUDAMED
    6 results · 17ms · 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.

    3I MODEL(S)7426 AND 7427 CELSEP CENTRIFUGE SYSTEM

    FDA 510(k)
    FDA Class 1 ·Clinical Chemistry

    PREVEN-A-STIK

    FDA 510(k)
    FDA Class 2 ·General Hospital

    MOD. FEMORAL COMP. NON-BEADED & BASIC ACE. SHELL

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    9900

    FDA Adverse Event
    Malfunction ·GE OEC MEDICAL SYSTEMS (SLC)·Product code JAA·February 13, 2013

    SPRINT FIDELIS

    FDA Adverse Event
    Death ·MEDTRONIC PUERTO RICO, INC.·Product code LWS·February 16, 2011

    TERUMO TCM 1 COOLING AND HEATING SYSEM

    FDA Adverse Event
    Malfunction ·TERUMO CARDIOVASCULAR SYSTEMS CORP.·Product code DWC·July 24, 2014