BEUDAMED
    8 results · 20ms · Sources: EU EUDAMED, US FDA

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    HEATED WIRE CIRCUITS FOR SCT 3000 HEATED HUMIDIFIER

    FDA 510(k)
    FDA Class 2 ·Anesthesiology

    MODIFICATION TO GUARDDOG OCCLUSION SYSTEM

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    DIO Medical IVA (ACIF, DLIF, PLIF, TLIF,and ALIF) Cage

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    LOOK

    FDA Adverse Event
    Other ·SURGICAL SPECIALTIES CORP. (DOING BUSINESS AS ANGIOTECH)·Product code GAM·February 20, 2007

    ANIMAS INSULIN INFUSION PUMP

    FDA Adverse Event
    Malfunction ·ANIMAS CORPORATION·Product code LZG·February 14, 2013

    CARPENTIER-EDWARDS PHYSIO II ANNULOPLASTY RING

    FDA Adverse Event
    Injury ·EDWARDS LIFESCIENCES·Product code KRH·January 17, 2011

    ULTRACISION HARMONIC ACE

    FDA Adverse Event
    Malfunction ·ETHICON ENDO-SURGERY, LLC.·Product code LFL·July 28, 2014

    Medtronic INTREPID Spinal System SPACER M 37X27, 12 DEG, Size: 10MM, Part Number: REF 7962210; 12MM, REF 7962212; 14MM, REF 7962214; 16MM, REF 7962216; 18MM, REF 7962218; 20MM, REF 7962220; USA, Rx only, STERILE R. The INTREPID Spinal System is indicated for use with autogenous bone graft in patients with degenerative disc disease.

    FDA Recall
    Terminated ·Medtronic Sofamor Danek USA Inc·Product code MAX·February 6, 2009