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

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    Cascadia Interbody System

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    Ophthalmic Ring

    FDA UDI
    KATENA PRODUCTS, INC.·00841668100813·FLIERINGA FIXATION RING 20MM

    External Fixation

    FDA UDI
    Life Spine, Inc.·00190837023256·85 Threaded Rod

    SANTORINI™ Corpectomy Cage System

    FDA UDI
    VB Spine LLC·10888857230576·Clip Inserter (Straight), Size 12x17 mm

    WEINMANNCOMPACT, MODEL WM 27380; WEINMANNCLICK2, MODEL WM 27340

    FDA 510(k)
    FDA Class 2 ·Anesthesiology

    AIDA VI.8 DIAGNOSTIC ULTRASOUND GM-72P00A, L13-5V1 TRANSDUCER

    FDA 510(k)
    FDA Class 2 ·Radiology

    9800

    FDA Adverse Event
    Malfunction ·GE OEC MEDICAL SYSTEMS INC.·Product code JAA·August 18, 2009

    ACRYSOF

    FDA Adverse Event
    Other ·ALCON RESEARCH, LTD./HUNTINGTON·Product code HQL·March 27, 2009

    8.5MM MEDULLARY REAMER HEAD

    FDA Adverse Event
    Malfunction ·SYNTHES (USA)·Product code HTO·June 18, 2009

    OXIMAX N-595 PULSE OXIMETER

    FDA Adverse Event
    Malfunction ·COVIDIEN, FORMERLY TYCOHEALTHCARE·Product code DQA·October 14, 2009

    ACRYSOF RESTOR

    FDA Adverse Event
    Other ·ALCON RESEARCH, LTD. / HUNTINGTON·Product code MFK·March 6, 2009

    ACRYSOF RESTOR

    FDA Adverse Event
    Other ·ALCON RESEARCH, LTD. / HUNTINGTON·Product code MFK·March 6, 2009

    9800

    FDA Adverse Event
    Malfunction ·GE OEC MEDICAL SYSTEMS (SLC)·Product code JAA·June 10, 2013

    UNICEL DXC 800 SYNCHRON SYSTEM

    FDA Adverse Event
    Malfunction ·BECKMAN COULTER, INC·Product code JJE·July 15, 2011

    LIFEPAK CR PLUS DEFIBRILLATOR

    FDA Adverse Event
    Malfunction ·PHYSIO-CONTROL, INC.·Product code MKJ·September 18, 2008

    PREMIUM SURGICLIP S-9.0 TITANIUM

    FDA Adverse Event
    Injury ·PONCE - USS·Product code GDO·August 19, 2009

    SPIDER CERVICAL PLATE SYSTEM

    FDA Adverse Event
    Injury ·X-SPINE SYSTEMS, INC.·Product code KWQ·September 17, 2009

    9600

    FDA Adverse Event
    Malfunction ·GE OEC MEDICAL SYSTEMS INC.·Product code JAA·August 18, 2009

    SPIDER CERVICAL PLATE SYSTEM

    FDA Adverse Event
    Injury ·X-SPINE SYSTEMS, INC.·Product code KWQ·September 17, 2009

    SPIDER CERVICAL PLATE SYSTEM

    FDA Adverse Event
    Injury ·X-SPINE SYSTEMS, INC.·Product code KWQ·September 17, 2009