BEUDAMED
    50 results · 28ms · Sources: EU EUDAMED, US FDA

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    Somatic Gene Mutation Detection System

    FDA Pre-Market Approval
    FDA Class 3 ·therascreen FGFR RGQ RT-PCR Kit

    Somatic Gene Mutation Detection System

    FDA Pre-Market Approval
    FDA Class 3 ·QIAGEN therascreen® FGFR RGQ RT-PCR Kit

    Somatic Gene Mutation Detection System

    FDA Pre-Market Approval
    FDA Class 3 ·therascreen FGFR RGQ RT-PCR Kit

    Somatic Gene Mutation Detection System

    FDA Pre-Market Approval
    FDA Class 3 ·therascreen FGFR RGQ PCR Kit

    Somatic Gene Mutation Detection System

    FDA Pre-Market Approval
    FDA Class 3 ·therascreen FGFR RGQ RT-PCR Kit

    Somatic Gene Mutation Detection System

    FDA Pre-Market Approval
    FDA Class 3 ·therascreen FGFR RGQ PCR Kit

    Somatic Gene Mutation Detection System

    FDA Pre-Market Approval
    FDA Class 3 ·QIAGEN therascreen® FGFR RGQ RT-PCR Kit

    Somatic Gene Mutation Detection System

    FDA Pre-Market Approval
    FDA Class 3 ·therascreen FGFR RGQ RT-PCR Kit

    Somatic Gene Mutation Detection System

    FDA Pre-Market Approval
    FDA Class 3 ·therascreen FGFR RGQ RT-PCR Kit

    Somatic Gene Mutation Detection System

    FDA Pre-Market Approval
    FDA Class 3 ·therascreen FGFR RGQ RT-PCR Kit

    SOL-M Syringe

    FDA UDI
    Sol-Millennium Medical, Inc.·00818392018172·SOL-M 3ml Luer Lock Syringe w/o Needle

    FINN KNEE SYSTEM

    FDA UDI
    Biomet Orthopedics, LLC·00880304268883·

    Protect U Guard Tie On Face Mask 3 Ply Green

    FDA UDI
    PROTECT U GUARD, LLC·B086100431·

    PILLING

    FDA UDI
    TELEFLEX INCORPORATED·14026704795298·

    Distraction Paddle - 11mm

    FDA UDI
    CAPTIVA SPINE, INC.·00850065741666·Distraction Paddle - 11mm

    Coaxial needle

    FDA UDI
    Möller Medical GmbH·04260277171919·

    Stent, Iliac

    FDA Pre-Market Approval
    FDA Class 3 ·OMNILINK ELITE PERIPHERAL BALLOON-EXPANDABLE STENT SYSTEM

    Analyzer, Medical Image

    FDA Pre-Market Approval
    FDA Class 2 ·QVCAD SYSTEM

    RESOLUTE ONYX RX

    FDA Adverse Event
    Malfunction ·MEDTRONIC IRELAND·Product code NIQ·January 31, 2019

    Stent, Iliac

    FDA Pre-Market Approval
    FDA Class 3 ·Omnilink Elite™ Vascular Balloon-Exoandable Stent System