BEUDAMED
    6 results · 20ms · 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 ×

    PERCUTANEOUS SURAPUBIC CATHETER

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

    Televere Podiatry X-Ray System HF

    FDA 510(k)
    FDA Class 2 ·Radiology

    CROSSER LP SYSTEM

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    TOTAL ASR ACET IMP SIZE 52

    FDA Adverse Event
    Injury ·DEPUY INTERNATIONAL LTD.-8010379·Product code KWA·April 30, 2014

    ENDOTAK RELIANCE

    FDA Adverse Event
    Malfunction ·CPI - DEL CARIBE·Product code NVY·October 10, 2012

    GORE EXCLUDER AAA ENDOPROSTHESIS

    FDA Adverse Event
    Injury ·W.L. GORE & ASSOCIATES·Product code MIH·July 26, 2010