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

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    Filters Regulation: Us FDA ×

    P.F.C. CRUCIATE RETAING KNEE SYSTEM

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    SIGMA

    FDA UDI
    DEPUY ORTHOPAEDICS, INC.·10603295245643·SIGMA RP STABILIZED TIBIAL INSERT TRIAL 2 25.0mm

    MODIFICATION TO DUREPAIR DURA REGENERATION MATRIX

    FDA 510(k)
    FDA Class 2 ·Neurology

    Alpha Pure

    FDA 510(k)
    FDA Class 2 ·Dental

    ONETOUCHPING GLUCOSEMGMTSYSTEM

    FDA Adverse Event
    Malfunction ·ANIMAS CORPORATION·Product code LZG·February 15, 2013

    ROTATING MULTIPLE CLIP APPLIER

    FDA Adverse Event
    Malfunction ·ETHICON ENDO-SURGERY, LLC.·Product code FZP·July 29, 2014

    OT ULTRA2 METER

    FDA Adverse Event
    Injury ·LIFESCAN INC.·Product code NBW·January 18, 2011

    TSH, THYROTROPIN

    FDA Adverse Event
    Malfunction ·ROCHE DIAGNOSTICS·Product code JLW·April 9, 2014

    TSH, THYROTROPIN

    FDA Adverse Event
    Malfunction ·ROCHE DIAGNOSTICS·Product code JLW·March 24, 2014

    FT4, FREE THYROXINE

    FDA Adverse Event
    Malfunction ·ROCHE DIAGNOSTICS·Product code CEC·February 20, 2014