BEUDAMED
    8 results · 28ms · Sources: EU EUDAMED, US FDA

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    BOVIE X-10 ELECTROSURGICAL GENERATOR(UNIT)

    FDA 510(k)
    FDA Class 2 ·General, Plastic Surgery

    ENDOBRONCHIAL TWIN LUMEN TUBE

    FDA 510(k)
    FDA Class 2 ·Anesthesiology

    MONITOR 5590- ANALYZER 5595EC

    FDA 510(k)
    FDA Class 2 ·Anesthesiology

    OT VERIO IQ METER

    FDA Adverse Event
    Malfunction ·LIFESCAN EUROPE, A DIVISION OF CILAG GMBH INTL·Product code NBW·June 3, 2014

    CUSTOM PAK

    FDA Adverse Event
    Injury ·ALCON - HOUSTON·Product code KYG·November 16, 2012

    RESTORE RECHARGEABLE NEUROSTIMULATOR

    FDA Adverse Event
    Injury ·MDT PUERTO RICO OPERATIONS CO., JUNCOS·Product code LGW·September 23, 2010

    BELLATEK ABUTMENT TSV 4.5MM

    FDA Adverse Event
    Malfunction ·ZIMMER DENTAL·Product code NHA·May 15, 2024

    KLS Martin Cranial Implants - MR Conditional; K944565: KLS-Martin Micro Osteosynthesis System (1.5MM); K971297: KLS Martin Centre-Drive Drill-Free Screw; K060177: KLS Martin Rigid Fixation - Sterile; K062570: Individual Patient Solutions - Ti (IPS-Ti); K072707: Individual Patient Solutions - PEEK (IPS-PEEK) ; K151382: Individual Patient Solutions - (IPS-PEEK) - STERILE

    FDA 510(k)
    FDA Class 2 ·Neurology