BEUDAMED
    25 results · 25ms · Sources: EU EUDAMED, US FDA

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    LiquiBand Plus

    FDA 510(k)
    FDA Class 2 ·General, Plastic Surgery

    Vanguard® Knee System

    FDA UDI
    Biomet Orthopedics, LLC·00880304271661·

    MCLEAN MEDICAL & SCIENTIFIC

    FDA registration
    MCLEAN MEDICAL & SCIENTIFIC·35 products·🇺🇸 United States

    INTEGRA CUSA NXT INFERIOR FOWARD BONE TIP

    FDA 510(k)
    FDA Unclassified ·Unknown

    U-RIGHT TD-4249/U-RIGHT TD-4250 BLOOD GLUCOSE MONITORING SYSTEM

    FDA 510(k)
    FDA Class 2 ·Clinical Chemistry

    STENOSCOP

    FDA Adverse Event
    Malfunction ·GE OEC MEDICAL SYSTEMS (SLC)·Product code JAA·July 11, 2011

    OT VERIO IQ METER

    FDA Adverse Event
    Malfunction ·LIFESCAN EUROPE, A DIVISION OF CILAG GMBH INTL·Product code NBW·June 22, 2013

    PARADIGM REAL-TIME REVEL INSULIN INFUSION PUMP

    FDA Adverse Event
    Injury ·MEDTRONIC MINIMED·Product code OYC·October 18, 2014

    TMJ SYSTEM LEFT STANDARD MANDIBULAR COMPONENT

    FDA Adverse Event
    Malfunction ·BIOMET MICROFIXATION·Product code LZD·November 8, 2018

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

    FDA Adverse Event
    Malfunction ·BIOMET MICROFIXATION·Product code JEY·November 8, 2018

    "2.4 MM" SYSTEM HIGH TORQUE (HT) CROSS-DRIVE SCREW, 2.7 X 12 MM

    FDA Adverse Event
    Malfunction ·BIOMET MICROFIXATION·Product code HWC·November 8, 2018

    TMJ SYSTEM RIGHT FOSSA COMPONENT, SMALL

    FDA Adverse Event
    Malfunction ·BIOMET MICROFIXATION·Product code LZD·November 8, 2018

    TMJ SYSTEM LEFT FOSSA COMPONENT, SMALL

    FDA Adverse Event
    Malfunction ·BIOMET MICROFIXATION·Product code LZD·November 8, 2018

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

    FDA Adverse Event
    Malfunction ·BIOMET MICROFIXATION·Product code HWC·November 8, 2018

    TMJ SYSTEM CROSS-DRIVE FOSSA SCREW, 2.0 X 9 MM

    FDA Adverse Event
    Malfunction ·BIOMET MICROFIXATION·Product code JEY·November 8, 2018

    TMJ SYSTEM RIGHT STANDARD MANDIBULAR COMPONENT

    FDA Adverse Event
    Injury ·BIOMET MICROFIXATION·Product code LZD·February 6, 2020

    TMJ SYSTEM CROSS DRIVE FOSSA SCREW

    FDA Adverse Event
    Injury ·BIOMET MICROFIXATION·Product code JEY·February 6, 2020

    TMJ SYSTEM LEFT FOSSA COMPONENT, SMALL

    FDA Adverse Event
    Injury ·BIOMET MICROFIXATION·Product code LZD·February 6, 2020

    2.4MM SYSTEM HIGH TORQUE (HT) CROSS-DRIVE SCREW

    FDA Adverse Event
    Injury ·BIOMET MICROFIXATION·Product code JEY·February 6, 2020

    TMJ SYSTEM CROSS DRIVE FOSSA SCREW

    FDA Adverse Event
    Injury ·BIOMET MICROFIXATION·Product code JEY·February 6, 2020