BEUDAMED
    12 results · 19ms · Sources: EU EUDAMED, US FDA

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    Filters Regulation: Us FDA ×

    BARD HYDROPHILIC COATED GUIDE WIRES

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    FIXED ELBOW 15M- FLIP TOP CAP - 22M/15F

    FDA UDI
    Intersurgical Incorporated·05030267058020·FIXED ELBOW 15M- FLIP TOP CAP - 22M/15F

    artegral life

    FDA UDI
    Merz Dental GmbH·D7091993000·anteriors; shade A1; mould CL

    Stainless Steel

    FDA UDI
    Seaspine Orthopedics Corporation·10889981114879·Rod Sterilization Case

    Vu aPod™ - L

    FDA UDI
    Seaspine Orthopedics Corporation·10889981118150·Vu aPod-L Instrument Case

    EMS PIEZON MASTER 700

    FDA 510(k)
    FDA Class 2 ·Dental

    Hexanium® ACIF

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    Proteus XR/a (SlOK : K993090)

    FDA Recall
    Open, Classified ·GE Healthcare, LLC·Product code KPR·August 9, 2019

    TAXUS® LIBERTÉ®

    FDA Adverse Event
    Injury ·BOSTON SCIENTIFIC - MAPLE GROVE·Product code NIQ·March 7, 2013

    PARADIGM REAL-TIME INSULIN INFUSION PUMP

    FDA Adverse Event
    Injury ·MEDTRONIC MINIMED·Product code MDS·February 7, 2011

    CAPSUREFIX NOVUS

    FDA Adverse Event
    Malfunction ·MPRI·Product code DTB·August 8, 2014

    Proteus XR/a (SlOK : K993090)

    FDA Enforcement
    Class II ·Ongoing·GE Healthcare, LLC·October 2, 2019