BEUDAMED
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    SPERM PREPARATION MEDIA

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

    P.F.C. SIGMA

    FDA UDI
    DEPUY ORTHOPAEDICS, INC.·10603295244653·P.F.C. SIGMA STABILIZED PLUS TIBIAL INSERT TRIA...

    SENSITITRE HAEMOPHILUS/STREPTOCOCCUS PNEUMONIAE (HP) MIC PLATE

    FDA 510(k)
    FDA Class 2 ·Microbiology

    SML-OSA2 Appliances

    FDA 510(k)
    FDA Class 2 ·Dental

    RIATA ST ACTIVE FIXATION

    FDA Adverse Event
    Malfunction ·ST JUDE MEDICAL CARDIAC RHYTHM MANAGEMENT DIVISION·Product code NVY·February 14, 2013

    PARADIGM REAL-TIME INSULIN INFUSION PUMP MMT - 722LNAB

    FDA Adverse Event
    Injury ·MEDTRONIC MINIMED·Product code MDS·January 11, 2011

    MECHANICAL (MANUAL) WHEELCHAIR

    FDA Adverse Event
    Malfunction ·INVAMEX·Product code IOR·July 29, 2014

    Medtronic INTREPID Spinal System SPACER M 37X27, 8 DEG, Size 10MM, Part Number: REF 7962810; 12MM, REF 7962812; 14MM, REF 7962814; 16MM, REF 7962816; 18MM, REF 7962818; 20MM, REF 7962820; 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