BEUDAMED
    3 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.

    Timberline Lateral Fusion System

    FDA UDI
    Highridge Medical, LLC·03662663255295·Case 5 Lat Rong & Impl Instr

    ARTERIAL CATHETER KIT

    FDA Adverse Event
    Injury ·ARGON MEDICAL DEVICES INC.·Product code GDY·February 19, 2019

    STELLAREX 0.035 OTW DRUG-COATED ANGIOPLASTY BALLOON

    FDA Adverse Event
    Injury ·SPECTRANETICS·Product code ONU·June 17, 2019