BEUDAMED
    10 results · 28ms · Sources: EU EUDAMED, US FDA

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    PULM O2 SUCTION CATHETER TRAYS

    FDA 510(k)
    FDA Class 1 ·Anesthesiology

    R82

    FDA UDI
    R82 A/S·05707292794833·

    ZIMMER AMBULATORY PUMP PAIN MANAGEMENT SYSTEMS WITH FENESTRATED CATHETER AND FLOW SPLITTER

    FDA 510(k)
    FDA Class 2 ·General Hospital

    Solex 7 Intravascular Heat Exchange Catheter, ZOLL Start-Up Kit

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    BONE ANCHOR SYSTEM FOR SOFT TISSUE SUPPORT

    FDA Adverse Event
    Injury ·BOSTON SCIENTIFIC - SPENCER·Product code MBI·April 27, 2012

    Wombat Living, Size 3, Item Numbers: 953121-00, 953126-00, 953131-00, 953132-00, 935-135-00, 935136-00, 953211-00, 953221-00, 953222-00, 953225-00, 953226-00, 953231-001, 953232-00, 953236-00 Product Usage: Activity chair (wheelchair)

    FDA Enforcement
    Class II ·Terminated·R82 A/S·May 22, 2019

    CAPSUREFIX MRI

    FDA Adverse Event
    Injury ·MPRI·Product code NVN·February 9, 2013

    RIATA ST OPTIM ACTIVE FIXATION

    FDA Adverse Event
    Death ·ST. JUDE MEDICAL, INC., CRMD·Product code NVY·July 23, 2014

    MECHANICAL (MANUAL) WHEELCHAIR

    FDA Adverse Event
    Malfunction ·TAIWAN AN I CO.,LTD.·Product code IOR·September 30, 2013

    Wombat Living, Size 3, Item Numbers: 953121-00, 953126-00, 953131-00, 953132-00, 935-135-00, 935136-00, 953211-00, 953221-00, 953222-00, 953225-00, 953226-00, 953231-001, 953232-00, 953236-00 Product Usage: Activity chair (wheelchair)

    FDA Recall
    Terminated ·Product code INM·March 28, 2019