BEUDAMED
    8 results · 27ms · Sources: EU EUDAMED, US FDA

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    MODIFICATION OF ENCORE LINEAR POROUS COATED HIP

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    Pro-Retractor Balfour Blade

    FDA UDI
    KOROS U.S.A., INC.·10840199542601·Pro-Retractor Balfour Blade Small 3 x 2-1/2"

    103 P37,BE ONLY,INLINE,STKR

    FDA UDI
    CURBELL MEDICAL PRODUCTS, INC.·00840828101059·103 P37,BE ONLY,INLINE,STKR

    TEN-YEAR FRACTURE RISK OPTION AND SIRI TABLE OPTION FOR NORLAND DXA BONE DENSITOMETERS

    FDA 510(k)
    FDA Class 2 ·Radiology

    EMPOWR Partial Knee

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    INTERSTIM II

    FDA Adverse Event
    Malfunction ·MEDTRONIC MED REL MEDTRONIC PUERTO RICO·Product code EZW·March 6, 2013

    SPRINT FIDELIS

    FDA Adverse Event
    Injury ·MPRI·Product code LWS·August 8, 2014

    SPRINT QUATTRO SECURE

    FDA Adverse Event
    Malfunction ·MEDTRONIC PUERTO RICO, INC.·Product code LWS·February 15, 2011