BEUDAMED
    9 results · 18ms · Sources: EU EUDAMED, US FDA

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    RANGEROLLER (MODIFIED)

    FDA 510(k)
    FDA Class 2 ·Physical Medicine

    Instrument Case

    FDA UDI
    KATENA PRODUCTS, INC.·00841668111055·SILICONE MAT FOR K 9-2320

    Instrument Case

    FDA UDI
    KATENA PRODUCTS, INC.·00841668110973·STERILIZING CASE MEDIUM/SMALL

    Arthrex®

    FDA UDI
    ARTHREX, INC.·00888867058699·POSTERIOR GLENOID RETRACTOR

    CONNECTED CARE MOBILE APPLICATION

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    L.A.M. IPM WOUND GEL

    FDA 510(k)
    FDA Unclassified ·Unknown

    KYPHX® HV-R¿ BONE CEMENT

    FDA Adverse Event
    Malfunction ·MEDTRONIC SPINE LLC·Product code NDN·December 10, 2010

    3.5MM LCP DISTAL TIBIA T-PLATE5 HOLES/90MM

    FDA Adverse Event
    Injury ·SYNTHES ELMIRA·Product code HRS·January 17, 2013

    UNIDENTIFIED ASR HEAD

    FDA Adverse Event
    Injury ·DEPUY INTERNATIONAL LTD.-8010379·Product code KXA·July 8, 2014