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

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    MODIFICATION OF REGULAR DIAMETER SINGLE STAGE (RDS) TPS DENTAL IMPLANT SYSTEM

    FDA 510(k)
    FDA Class 2 ·Dental

    Medichoice

    FDA UDI
    OWENS & MINOR DISTRIBUTION, INC.·10885632106132·Sphygmomanometer Aneroid Blood Pressure Deluxe ...

    Masel

    FDA UDI
    Ortho Organizers, Inc.·00190707035839·.016 X .022 Upper Stainless Steel Resilient Int...

    AMK MODULAR TIBIAL WEDGE SYSTEM

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    TECNOL SILK STRIP

    FDA 510(k)
    FDA Class 1 ·General Hospital

    IMPL-HOLDER F/SYNFIX-LR

    FDA Adverse Event
    Malfunction ·SYNTHES GMBH·Product code LXH·March 8, 2013

    QUICKSET TPRD HEX SCDR U-JOINT

    FDA Adverse Event
    Malfunction ·DEPUY ORTHOPAEDICS, INC.·Product code LXH·August 8, 2014

    SYBRONPRO TL

    FDA Adverse Event
    Injury ·EBI INC.·Product code DZE·February 16, 2011

    ZILVER PTX 35 DRUG-ELUTING STENT

    FDA Adverse Event
    Injury ·COOK IRELAND LTD·Product code NIU·July 14, 2016

    ZILVER PTX 35 DRUG-ELUTING STENT

    FDA Adverse Event
    Injury ·COOK IRELAND LTD·Product code NIU·November 23, 2015