BEUDAMED
    7 results · 25ms · 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.

    DRAGER-VAPOR 19.1 W/PLUG SYSTEM S PLUS

    FDA 510(k)
    FDA Class 2 ·Anesthesiology

    Polystar Selection EDITION

    FDA UDI
    Merz Dental GmbH·D7091981472·anteriors; shade BL2; mould BIM4

    SMARTPORT CT VORTEX; LP TITANIUM, SINGLE PLASTIC, SINGLE TITANIUM, TRIUMPH LOW PROFILE TITANIUM PORTS

    FDA 510(k)
    FDA Class 2 ·General Hospital

    AEROFLEX(TM) Automatic Endoscope Reprocessor with AUTOSURE(TM) MRC Monitor

    FDA 510(k)
    FDA Class 2 ·Gastroenterology, Urology

    APEX HOLE ELIM POSITIVE STOP

    FDA Adverse Event
    Injury ·DEPUY WARSAW·Product code LPH·February 27, 2013

    9900

    FDA Adverse Event
    Malfunction ·GE OEC MEDICAL SYSTEMS (SLC)·Product code JAA·February 1, 2011

    OPTETRAK 3 PEG PATELLA, CEMENTED

    FDA Adverse Event
    Malfunction ·EXACTECH, INC·Product code JWH·July 25, 2014