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

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    RYDER CONTACT LENS CASE

    FDA 510(k)
    FDA Class 2 ·Ophthalmic

    Splashwire Hydrophilic Guide Wire (MSWSTD35180J1O5); Splashwire Hydrophilic Guide Wire (MSWSTD35260J1O5); Splashwire Hydrophilic Guide Wire (MSWSTDA35150LT); Splashwire Hydrophilic Guide Wire (MSWSTFA35260LT); Splashwire Hydrophilic Guide Wire (MSWSTFA35150LT); Splashwire Hydrophilic Guide Wire (MSWSTFS38150LT)

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    CUSTOM-HIP TOOL

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    E1 RINGLOC BIPOLAR 28X51MM

    FDA Adverse Event
    Malfunction ·ZIMMER BIOMET, INC.·Product code LZO·June 17, 2019

    BIOMEX SHELL PC DIA48MM LN 22

    FDA Adverse Event
    Injury ·BIOMET UK LTD.·Product code LZO·December 2, 2015

    OT VERIO IQ METER

    FDA Adverse Event
    Malfunction ·LIFESCAN EUROPE, A DIVISION OF CILAG GMBH INTL·Product code NBW·February 8, 2013

    COLLEAGUE CX TRIPLE CHANNEL VOLUMETRIC INFUSION PUMP

    FDA Adverse Event
    Malfunction ·BAXTER HEALTHCARE - SINGAPORE·Product code FRN·January 6, 2011

    COGNIS

    FDA Adverse Event
    Injury ·GUIDANT CRM CLONMEL IRELAND·Product code LWP·July 22, 2014