BEUDAMED
    8 results · 19ms · 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 ×

    CMS CRANIO MAXILLO FACIAL TITANIUM IMPLANT SYSTEM

    FDA 510(k)
    FDA Class 2 ·Dental

    De Soutter Medical

    FDA UDI
    DE SOUTTER MEDICAL LIMITED·05051471122376·K-WIRE - SINGLE TROCAR THREADED 1.6mm DIA x 230mm

    Unimed Reusable SpO2 Sensors (-08 Series) (U403S-08); Unimed Reusable SpO2 Sensors (-08 Series) (U203S-08); Unimed Reusable SpO2 Sensors (-08 Series) (U103S-08); Unimed Reusable SpO2 Sensors (-08 Series) (U103-08)

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    MINIMATE COMPRESSOR

    FDA 510(k)
    FDA Class 2 ·Anesthesiology

    TT (TRACHEOSTOMY TUBES)

    FDA Adverse Event
    Malfunction ·Product code BTR·October 24, 2017

    CAPSURE SP NOVUS

    FDA Adverse Event
    Injury ·MPRI·Product code DTB·February 9, 2013

    OT VERIO IQ METER

    FDA Adverse Event
    Malfunction ·LIFESCAN EUROPE, A DIVISION OF CILAG GMBH INTL·Product code NBW·July 23, 2014

    SPRINT FIDELIS

    FDA Adverse Event
    Death ·MEDTRONIC PUERTO RICO, INC.·Product code LWS·January 6, 2011