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

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    PERKINS HAND-HELD APPLANATION TONOMETER

    FDA 510(k)
    FDA Class 2 ·Ophthalmic

    P.F.C. SIGMA

    FDA UDI
    DEPUY ORTHOPAEDICS, INC.·10603295239277·P.F.C. SIGMA TC3 TIBIAL INSERT TRIAL SZ 2 15mm ...

    EMDS, CK/CK-MB VERIFIER, ITEM NUMBER 67---/95

    FDA 510(k)
    FDA Class 1 ·Clinical Chemistry

    L SOPHIA

    FDA 510(k)
    FDA Unclassified ·Unknown

    ASR UNI FEMORAL IMPL SIZE 45

    FDA Adverse Event
    Injury ·DEPUY INTERNATIONAL·Product code KWA·February 14, 2013

    AC POWER MODULE

    FDA Adverse Event
    Malfunction ·PHILIPS HEALTHCARE·Product code MKJ·January 10, 2011

    ACCU-CHEK ® SPIRIT COMBO

    FDA Adverse Event
    Malfunction ·ROCHE DIAGNOSTICS·Product code LZG·July 28, 2014