BEUDAMED
    8 results · 16ms · Sources: EU EUDAMED, US FDA

    Get notified when this changes

    We'll email you when new records match this search — new devices, new clearances, certificate changes, or withdrawals.
    Filters Status: Injury ×

    ELEVATE PROLAPSE REPAIR SYSTEM

    FDA Adverse Event
    Injury ·AMERICAN MEDICAL SYSTEMS, INC.·Product code OTP·January 28, 2013

    "2.7MM" SYSTEM EMERGENCY CROSS DRIVE SCREW, 1/PKG

    FDA Adverse Event
    Injury ·BIOMET MICROFIXATION·Product code HWC·October 25, 2018

    TMJ SYSTEM LEFT FOSSA COMPONENT, SMALL

    FDA Adverse Event
    Injury ·BIOMET MICROFIXATION·Product code LZD·October 25, 2018

    "2.4 MM" SYSTEM HIGH TORQUE (HT) CROSS-DRIVE SCREW, 2.7 X 10 MM

    FDA Adverse Event
    Injury ·BIOMET MICROFIXATION·Product code HWC·October 25, 2018

    TMJ SYSTEM CROSS DRIVE FOSSA SCREW, 2.0 X 9 MM

    FDA Adverse Event
    Injury ·BIOMET MICROFIXATION·Product code JEY·October 25, 2018

    "2.4MM" SYSTEM HIGH TORQUE (HT)CROSS-DRIVE SCREW, 2.7X8MM

    FDA Adverse Event
    Injury ·BIOMET MICROFIXATION·Product code HWC·October 25, 2018

    TMJ SYSTEM CROSS-DRIVE FOSSA SCREW, 2.0 X 7 MM

    FDA Adverse Event
    Injury ·BIOMET MICROFIXATION·Product code JEY·October 25, 2018

    "2.7MM" SYSTEM EMERGENCY CROSS DRIVE SCREW, 1/PKG

    FDA Adverse Event
    Injury ·BIOMET MICROFIXATION·Product code HWC·October 25, 2018