BEUDAMED
    24 results · 24ms · Sources: EU EUDAMED, US FDA

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    Arthrex Eclipse Shoulder Prosthesis System

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    EarQ

    FDA UDI
    Oticon A/S·05707131350831·G40 S, BTE PP 13 2.4G 105 C090 EARQ

    Lockheed - 18 Metal

    FDA UDI
    Certified Safety Manufacturing, Inc.·00766588015026·Lockheed - 18 Metal

    16PW - Washington Gas - Poly White

    FDA UDI
    Certified Safety Manufacturing, Inc.·00766588014425·16PW - Washington Gas - Poly White

    ADC DENTAL

    FDA 510(k)
    FDA Class 2 ·Dental

    HEADWAY 17 ADVANCED MICROCATHETER

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    GORE VIABAHN® ENDOPROSTHESIS

    FDA Adverse Event
    Injury ·W.L. GORE & ASSOCIATES·Product code JCT·July 30, 2015

    GORE HEMOBAHN® ENDOPROSTHESIS

    FDA Adverse Event
    Injury ·W.L. GORE & ASSOCIATES·Product code NIP·July 30, 2015

    GORE EXCLUDER AAA ENDOPROSTHESIS

    FDA Adverse Event
    Injury ·W. L. GORE & ASSOCIATES,·Product code MIH·October 17, 2008

    OCTRODE LEAD

    FDA Adverse Event
    Malfunction ·ST. JUDE MEDICAL - NEUROMODULATION·Product code LGW·August 4, 2011

    ONETOUCHPING GLUCOSEMGMTSYSTEM

    FDA Adverse Event
    Injury ·ANIMAS CORPORATION·Product code LZG·July 2, 2013

    REVEAL XT

    FDA Adverse Event
    Injury ·MEDTRONIC, INC.·Product code DSI·December 9, 2016

    ESSURE

    FDA Adverse Event
    Injury ·BAYER PHARMA AG·Product code HHS·August 7, 2024

    ESSURE

    FDA Adverse Event
    Injury ·BAYER PHARMA AG·Product code HHS·August 7, 2024

    IMPLANTABLE INFUSION PUMP

    FDA Adverse Event
    Malfunction ·MEDTRONIC NEUROMODULATION·Product code LKK·January 8, 2016

    SCREW,FIXATION,BONE

    FDA Adverse Event
    Injury ·OBERDORF SYNTHES PRODUKTIONS GMBH·Product code HWC·January 7, 2019

    PLATE,FIXATION,BONE

    FDA Adverse Event
    Injury ·OBERDORF SYNTHES PRODUKTIONS GMBH·Product code HRS·January 7, 2019

    SCREW,FIXATION,BONE

    FDA Adverse Event
    Injury ·OBERDORF SYNTHES PRODUKTIONS GMBH·Product code HWC·January 7, 2019

    PLATE,FIXATION,BONE

    FDA Adverse Event
    Injury ·OBERDORF SYNTHES PRODUKTIONS GMBH·Product code HRS·January 7, 2019

    CROWN PRT PERICARDIAL HEART VALVE

    FDA Adverse Event
    Injury ·LIVANOVA CANADA CORP·Product code LWR·June 7, 2018