BEUDAMED
    8 results · 27ms · Sources: EU EUDAMED, US FDA

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    ANCHORLOK RL SOFT TISSUE ANCHOR SYSTEM

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    PERSONALLY(TM), MODEL 241 SIZES 0-12,LEFT & RIGHT

    FDA 510(k)
    FDA Class 1 ·General, Plastic Surgery

    TARGET THERAPEUTICS COILS

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    UNKNOWN PRODUCT - SET SCREW

    FDA Adverse Event
    Injury ·STRYKER OSTEOSYNTHESIS KIEL·Product code HWC·October 12, 2012

    9900

    FDA Adverse Event
    Malfunction ·GE OEC MEDICAL SYSTEMS (SLC)·Product code JAA·June 19, 2014

    VIRTUOSO DR

    FDA Adverse Event
    Injury ·IPG MFG SWITZERLAND·Product code LWS·February 15, 2013

    COATED VICRYL RAPIDE (POLYGLACTIN 910) SUTURE

    FDA Adverse Event
    Malfunction ·ETHICON, INC.·Product code GAM·December 23, 2010

    Custom Pack, part number AMS4776 Custom Pack, part number AMS4776(A Custom Pack, part number AMS5643 Custom Pack, part number AMS5643(A Custom Pack, part number AMS6012 Custom Pack, part number AMS6383 Custom Pack, part number PSS2135(B Custom Pack, part number PSS2798(B Custom Pack, part number PSS2798(C Custom Pack, part number PSS3463

    FDA Enforcement
    Class II ·Terminated·Windstone Medical Packaging, Inc.·March 8, 2017