BEUDAMED
    16 results · 32ms · Sources: EU EUDAMED, US FDA

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    MAGNESIUM QVET

    FDA 510(k)
    FDA Class 1 ·Clinical Chemistry

    Vista Solution® 30-day Monitoring Kit

    FDA UDI
    Vital Connect, Inc.·00850490007252·Vista Solution® 30-day Monitoring Kit

    SILVERLON ISLAND WOUND DRESSING, SILVERLON WOUND PAD DRESSING

    FDA 510(k)
    FDA Unclassified ·Unknown

    MX POLYAXIAL PEDICLE SCREW

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    ACCU-CHEK SPIRIT

    FDA Adverse Event
    Malfunction ·ROCHE HEALTH SOLUTIONS INC.·Product code LZG·January 18, 2013

    INTERLINK CONTINU-FLO 4-WAY STOPCOCK EXT SET

    FDA Adverse Event
    Malfunction ·BAXTER HEALTHCARE - AIBONITO·Product code FMG·December 30, 2010

    PARADIGM REAL-TIME REVEL INSULIN INFUSION PUMP

    FDA Adverse Event
    Malfunction ·MEDTRONIC PUERTO RICO OPERATIONS CO.·Product code OYC·July 17, 2014

    ORTHOSIS, SPONDYLOSTHESIS SPINAL FIXATION

    FDA Adverse Event
    Injury ·WRIGHTS LANE SYNTHES USA PRODUCTS LLC·Product code MNH·May 1, 2019

    ORTHOSIS, SPONDYLOSTHESIS SPINAL FIXATION

    FDA Adverse Event
    Injury ·WRIGHTS LANE SYNTHES USA PRODUCTS LLC·Product code MNH·May 1, 2019

    ORTHOSIS, SPONDYLOSTHESIS SPINAL FIXATION

    FDA Adverse Event
    Injury ·WRIGHTS LANE SYNTHES USA PRODUCTS LLC·Product code MNH·May 1, 2019

    SCREW,FIXATION,BONE

    FDA Adverse Event
    Injury ·WRIGHTS LANE SYNTHES USA PRODUCTS LLC·Product code HWC·May 1, 2019

    ORTHOSIS, SPONDYLOSTHESIS SPINAL FIXATION

    FDA Adverse Event
    Injury ·WRIGHTS LANE SYNTHES USA PRODUCTS LLC·Product code MNH·May 1, 2019

    SCREW,FIXATION,BONE

    FDA Adverse Event
    Injury ·WRIGHTS LANE SYNTHES USA PRODUCTS LLC·Product code HWC·May 1, 2019

    MegaPower Electrosurgical Generator, Product code 1000, GTIN 10614559103715

    FDA Enforcement
    Class II ·Terminated·Megadyne Medical Products, Inc.·August 22, 2018

    Reamer / Irrigator / Aspirator (RIA): RIA Drive Shafts, RIA Tube Assemblies, sterile, RIA Reamer Head, sterile (12.0mm-19.0mm); intended to clear the medullary canal of bone marrow and debris and to effectively size the medullary canal for the acceptance of an intramedullary implant or prosthesis

    FDA Enforcement
    Class II ·Terminated·Synthes, Inc.·July 22, 2015

    Alcon Custom Pak

    FDA Enforcement
    Class II ·Ongoing·Alcon Research, LTD.·August 23, 2023