BEUDAMED
    7 results · 19ms · Sources: EU EUDAMED, US FDA

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    N-395 PULSE OXIMETER, WITH EXTENDED DEVICE CLAIMS

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    artegral life

    FDA UDI
    Merz Dental GmbH·D7091993637·anteriors; shade BL4; mould BIL

    MRH ALFA Radiographic System, MRH II Radiographic System, MRH IIE Radiographic System

    FDA 510(k)
    FDA Class 2 ·Radiology

    JMS BLUNT A. V. FISTULA NEEDLE SET WITH SITE PREPARATION TOOL MODEL 820-5300, 820-6300 AND 820-7300

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

    TECNIS ITEC PRELOADED 1-PIECE IOL

    FDA Adverse Event
    Malfunction ·ABBOTT MEDICAL OPTICS·Product code HQL·March 7, 2013

    ISERT ASPHERIC INTRAOCULAR LENS

    FDA Adverse Event
    Malfunction ·HOYA SURGICAL OPTICS, INC.·Product code HQL·January 6, 2011

    CAPSUREFIX NOVUS

    FDA Adverse Event
    Injury ·MPRI·Product code DTB·August 8, 2014