BEUDAMED
    11 results · 22ms · Sources: EU EUDAMED, US FDA

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    Reveal LINQ

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    Ophthalmic Speculum

    FDA UDI
    KATENA PRODUCTS, INC.·00841668100073·TEMPORAL SPECULUM SOLID BLADES

    HNM Women Care

    FDA UDI
    HNM STAINLESS, LLC.·00812171028116·PESSARY, DISH #1, W/O SUPPORT, 55mm

    HALLMARK ANTERIOR CERVCIAL PLATE SYSTEM, HALLMARK FIVE-LEVEL CERVICAL PLATES

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    MUSE CARDIOLOGY INFORMATION SYSTEM

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    10MM INZII RETRIEVAL SYSTEM 10/BOX

    FDA Adverse Event
    APPLIED MEDICAL·Product code GCJ·November 16, 2011

    OT VERIO FLEX METER

    FDA Adverse Event
    Malfunction ·LIFESCAN EUROPE, A DIVISION OF CILAG GMBH INTL·Product code NBW·April 1, 2015

    OT VERIO IQ METER

    FDA Adverse Event
    Malfunction ·LIFESCAN EUROPE, A DIVISION OF CILAG GMBH INTL·Product code NBW·October 8, 2014

    ACCESS

    FDA Adverse Event
    Malfunction ·BAXTER HEALTHCARE - MALTA·Product code FPA·June 6, 2013

    TERUMO VIRTUOSAPH VEIN HARVESTING SYSTEM

    FDA Adverse Event
    Malfunction ·TERUMO CARDIOVASCULAR SYSTEMS CORP.·Product code GCJ·June 22, 2011

    TREVO XP PROVUE 4MM X 30MM

    FDA Adverse Event
    Injury ·STRYKER NEUROVASCULAR-UTAH-SALT LAKE CITY·Product code NRY·July 24, 2020