BEUDAMED
    7 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 ×

    RadiForce MX217

    FDA 510(k)
    FDA Class 2 ·Radiology

    Philips

    FDA UDI
    Sbo Hearing A/S·05714464032631·HEARLINK 7030 MNR T BR/TP

    PHILIPS HEARTSTART FR3 AUTOMATED EXTERNAL DEFIBRILLATOR

    FDA 510(k)
    FDA Class 3 ·Cardiovascular

    SCOPE GUARD PROTECTIVE SHEATH, MODEL TEL-SH

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

    DIALYZER, HIGH PERMEABILITY WITH OR WITHOUT SEALED DIALYSATE SYSTEM

    FDA Adverse Event
    Injury ·BAXTER HEALTHCARE CORPORATION·Product code KDI·November 6, 2014

    ISOLINE

    FDA Adverse Event
    Injury ·SORIN CRM·Product code MRM·August 12, 2011

    ASR ACETABULAR CUPS 56

    FDA Adverse Event
    Injury ·DEPUY INTL., LTD. - 8010379·Product code KWA·July 16, 2013