BEUDAMED
    11 results · 21ms · Sources: EU EUDAMED, US FDA

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    SYNTHES CARNIOFACIAL PLATE AND SCREW SYSTEM

    FDA 510(k)
    FDA Class 2 ·Dental

    Silicone Face Mask

    FDA UDI
    MERCURY ENTERPRISES, INC.·10641043506080·

    InTess Lumbar Cage

    FDA UDI
    Kalitec Direct LLC·B07312K0106080·Trial, 26 x 8mm, 8 Degree, Tapered, Straight

    SUCTION VASCULAR STAPLER AND IMPLANTABLE STAPLE SYSTEM

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

    MODIFICATION TO LAP TOP VENTILATOR (LTV)

    FDA 510(k)
    FDA Class 2 ·Anesthesiology

    ZILVER 518 BILIARY SELF-EXPANDING STENT

    FDA Adverse Event
    Malfunction ·COOK IRELAND LTD·Product code FGE·September 21, 2017

    LNOP MP12 PATIENT CABLE

    FDA Adverse Event
    Malfunction ·MASIMO CORPORATION·Product code DQA·May 15, 2015

    EASYPUMP II ST 100-0, 5-S

    FDA Adverse Event
    Malfunction ·B. BRAUN MEDICAL PRODUCTION LTD.·Product code MEB·March 13, 2013

    PATELLA CALIPER

    FDA Adverse Event
    Malfunction ·STRYKER ORTHOPAEDICS MAHWAH·Product code LXH·March 15, 2011

    QUICKSITE LV

    FDA Adverse Event
    Injury ·ST JUDE MEDICAL CARDIAC RHYTHM MANAGEMENT DIVISION·Product code DXY·May 27, 2008

    ZILVER 518 SELF-EXPANDING STENT

    FDA Adverse Event
    Malfunction ·COOK IRELAND LTD·Product code FGE·October 26, 2012