BEUDAMED
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    STERITEC CROSS-CHECKS

    FDA 510(k)
    FDA Class 2 ·General Hospital

    KMEDIC

    FDA UDI
    TELEFLEX INCORPORATED·24026704286397·

    AUTO SUTURE MODIFIED ENDO STREAM SUC./IRRI. DEVICE

    FDA 510(k)
    FDA Class 2 ·Obstetrics/Gynecology

    MEDICAL SUNLAMP FOR PHOTOTHERAPY

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

    PCA PLS II

    FDA Adverse Event
    Malfunction ·HOSPIRA COSTA RICA LTD.·Product code MEA·June 12, 2014

    PROTECTA XT CRT-D

    FDA Adverse Event
    Injury ·MEDTRONIC MED REL MEDTRONIC PUERTO RICO·Product code NIK·February 11, 2013

    TENDRIL ST

    FDA Adverse Event
    Injury ·ST JUDE MEDICAL CARDIAC RHYTHM MANAGEMENT DIVISION·Product code DTB·January 10, 2011