BEUDAMED
    14 results · 22ms · Sources: EU EUDAMED, US FDA

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    ReliOn Premier Classic Blood Glucose Monitoring System

    FDA 510(k)
    FDA Class 2 ·Clinical Chemistry

    APEX Knee System

    FDA UDI
    Omni Life Science, Inc.·00841690198567·AK3 Ultra Insert Trial Size 2, 20mm

    EXPERIENCE®

    FDA UDI
    Gc Orthodontics America Inc.·D78819222000201·EXMRC MBT 022/UL2 10T 8A

    EXPERIENCE®

    FDA UDI
    Gc Orthodontics America Inc.·D78819222000101·EXMRC ROTH 022/UL2 8T 9A

    EXPERIENCE

    FDA UDI
    Gc Orthodontics America Inc.·D78819222000071·Exp CCO RH 022/UL2 10T 9A

    Responsive Orthopedics Total Knee Arthroplasty System

    FDA UDI
    RESPONSIVE ORTHOPEDICS, LLC·00841973108023·TRIAL 90-SRK-192220 POLY-MPCS 2X20 LEFT

    ENI-EYE SH SOFT K SEMI SCLERAL (EFROFILCON A) SOFT (HYDROPHILIC) KERATOCONUS AND IRREGULAR COR ENI-EYE SH SOFT K TORIC S

    FDA 510(k)
    FDA Class 2 ·Ophthalmic

    DEVILBISS INTELLIPAP / SLEEPCUBE AUTO BILEVEL

    FDA 510(k)
    FDA Class 2 ·Anesthesiology

    SCREW, FIXATION, BONE

    FDA Adverse Event
    Injury ·SYNTHES USA·Product code HWC·August 8, 2017

    8800

    FDA Adverse Event
    Malfunction ·GE OEC MEDICAL SYSTEMS (SLC)·Product code JAA·June 20, 2013

    ZEPHYR XL DR

    FDA Adverse Event
    Malfunction ·ST. JUDE MEDICAL, INC., CRMD·Product code LWP·January 13, 2014

    OT ULTRALINK METER

    FDA Adverse Event
    Malfunction ·LIFESCAN INC.·Product code NBW·August 4, 2011

    5.0MM TI LOCKING HEAD SCREW SELF-TAPPING 75MM

    FDA Adverse Event
    Injury ·SYNTHES BETTLACH·Product code KTT·August 8, 2017

    TRUE METRIX AIR

    FDA Adverse Event
    Malfunction ·TRIVIDIA HEALTH INC·Product code NBW·June 18, 2020