BEUDAMED
    289 results · 35ms · Sources: EU EUDAMED, US FDA

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    CUSA EXCEL 36KHZ CURVED EXTENDED STANDARDTIP

    FDA Adverse Event
    Malfunction ·INTEGRA LIFESCIENCES(IRELAND)·Product code LFL·July 15, 2020

    SURPASS EVOLVE 3.25MM X 17MM - IDE

    FDA Adverse Event
    Injury ·STRYKER NEUROVASCULAR CORK·Product code OUT·September 4, 2024

    SURPASS EVOLVE 4.0MM X 12MM - IDE

    FDA Adverse Event
    Injury ·STRYKER NEUROVASCULAR CORK·Product code OUT·September 5, 2024

    SURPASS EVOLVE 4.0MM X 17MM - IDE

    FDA Adverse Event
    Injury ·STRYKER NEUROVASCULAR CORK·Product code OUT·September 9, 2024

    CUSA EXCEL 36KHZ CURVED EXTENDED STANDARDTIP

    FDA Adverse Event
    Malfunction ·INTEGRA LIFESCIENCES(IRELAND)·Product code LFL·July 15, 2020

    SURPASS EVOLVE 4.0MM X 17MM - IDE

    FDA Adverse Event
    Injury ·STRYKER NEUROVASCULAR CORK·Product code OUT·September 9, 2024

    SURPASS EVOLVE 3.25MM X 12MM - IDE

    FDA Adverse Event
    Injury ·STRYKER NEUROVASCULAR CORK·Product code OUT·September 6, 2024

    COBAS 8000 C502 MODULE

    FDA Adverse Event
    Malfunction ·ROCHE DIAGNOSTICS·Product code JJE·October 14, 2014

    TENSION FREE VAGINAL TAPE

    FDA Adverse Event
    Injury ·ETHICON INC·Product code OTN·June 14, 2013

    NAVILYST MEDICAL / XCELA

    FDA Adverse Event
    Injury ·NAVILYST MEDICAL·Product code LJS·July 13, 2011

    UNKNOWN_NEUROVASCULAR_PRODUCT

    FDA Adverse Event
    Injury ·STRYKER NEUROVASCULAR CORK·Product code OUT·January 20, 2020

    Implantable Cardioverter Defibrillator (Non-Crt)

    FDA Pre-Market Approval
    FDA Class 3 ·SUBCUTANEOUS IMPLANTABLE DEFIBRILLATOR (S-ICD) SYSTEM

    Kit, Rna Detection, Human Papillomavirus

    FDA Pre-Market Approval
    FDA Class 3 ·APTIMA HPV ASSAY

    UNKNOWN (SURPASS STREAMLINE)

    FDA Adverse Event
    Malfunction ·STRYKER NEUROVASCULAR CORK·Product code OUT·December 16, 2019

    Philips Evolution Upgrade 1.5T with MR Elastography (MRE). 1. Model Number (REF): 782116 2. Model Number (REF): 782148. 3. Model Number (REF): 782166.

    FDA Enforcement
    Class II ·Ongoing·Philips North America·May 6, 2026

    UNKNOWN_NEUROVASCULAR_PRODUCT

    FDA Adverse Event
    Malfunction ·STRYKER NEUROVASCULAR CORK·Product code OUT·December 23, 2019

    UNKNOWN (SURPASS STREAMLINE)

    FDA Adverse Event
    Injury ·STRYKER NEUROVASCULAR CORK·Product code OUT·June 4, 2019

    UNKNOWN_NEUROVASCULAR_PRODUCT

    FDA Adverse Event
    Malfunction ·STRYKER NEUROVASCULAR CORK·Product code OUT·April 1, 2020

    UNKNOWN_NEUROVASCULAR_PRODUCT

    FDA Adverse Event
    Malfunction ·STRYKER NEUROVASCULAR CORK·Product code OUT·April 29, 2020

    UNKNOWN (SURPASS STREAMLINE)

    FDA Adverse Event
    Injury ·STRYKER NEUROVASCULAR CORK·Product code OUT·June 28, 2019