BEUDAMED
    15 results · 20ms · Sources: EU EUDAMED, US FDA

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    MODEL 110-5 & 140-8

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    DD cubeY® HL

    FDA UDI
    Dental Direkt GmbH·EDDIG8420051·The DD cubeY® HL zirconium dioxide milling blan...

    SpineFab Vertebral Body Replacement (VBR) System

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    ACHTUNG TD-4207, CLEVER CHEK TD-4209, CLEVER CHEK TD-4222

    FDA 510(k)
    FDA Class 2 ·Clinical Chemistry

    NA

    FDA UDI
    Zimmer, Inc.·00889024193666·

    NA

    FDA UDI
    Zimmer, Inc.·00889024193673·

    OT VERIO IQ METER

    FDA Adverse Event
    Malfunction ·LIFESCAN EUROPE, A DIVISION OF CILAG GMBH INTL·Product code NBW·May 31, 2014

    ACRYSOF

    FDA Adverse Event
    Injury ·ALCON RESEARCH, LTD./HUNTINGTON·Product code HQL·November 14, 2012

    REPAIR SYSTEM 5 SAGITTAL SAW

    FDA Adverse Event
    Malfunction ·STRYKER INSTRUMENTS KALAMAZOO·Product code KIJ·August 26, 2010

    NV MICROCATHETER

    FDA Adverse Event
    Injury ·COVIDIEN (IRVINE)·Product code KRA·April 24, 2017

    ONYX

    FDA Adverse Event
    Injury ·COVIDIEN (IRVINE)·Product code MFE·April 24, 2017

    ONYX

    FDA Adverse Event
    Injury ·COVIDIEN (IRVINE)·Product code MFE·April 24, 2017

    NV MICROCATHETER

    FDA Adverse Event
    Malfunction ·COVIDIEN (IRVINE)·Product code KRA·April 24, 2017

    ONYX LES

    FDA Adverse Event
    Malfunction ·COVIDIEN (IRVINE)·Product code MFE·April 24, 2017

    ON-X PROSTHETIC HEART VALVE

    FDA Adverse Event
    Injury ·CRYOLIFE, INC.·Product code LWQ·September 25, 2019