BEUDAMED
    7 results · 33ms · Sources: EU EUDAMED, US FDA

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    DETERMINATION OF MAGNESIUM IN SERUM OR

    FDA 510(k)
    FDA Class 1 ·Clinical Chemistry

    UniTip High Resolution Catheter

    FDA UDI
    Unisensor AG·07640172973578·

    Amplatz Goose Neck Snare Kit

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    GRYPHON BR ANCHOR WITH PERMACORD, GRYPHON BR DS ANCHOR WITH PERMACORD,GRYPHON PEEK ANCHOR WITH PERMACORD, GRYPHON PEEK

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    VA-LCP-2-COLUMN DRP2.4 VOLAR LE SHAFT 3H

    FDA Adverse Event
    Malfunction ·SYNTHES GMBH·Product code HRS·November 21, 2012

    PARADIGM REAL-TIME REVEL INSULIN INFUSION PUMP

    FDA Adverse Event
    Malfunction ·MEDTRONIC PUERTO RICO OPERATIONS CO.·Product code OYC·June 12, 2015

    COLLAMER ULTRAVIOLET-ABSORBING POSTERIOR CHAMBER THREE PIECE FOLDABLE INTRAOCULA

    FDA Adverse Event
    Malfunction ·STAAR SURGICAL COMPANY·Product code HQL·September 15, 2010