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

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    Separator, Automated, Blood Cell And Plasma, Therapeutic

    FDA Pre-Market Approval
    FDA Unclassified ·COBE CENTRY(R) TPE SYSTEM

    Separator, Automated, Blood Cell And Plasma, Therapeutic

    FDA Pre-Market Approval
    FDA Unclassified ·COBE CENTRY(R) TPE SYSTEM

    Titanium Universal Abutment

    FDA UDI
    T.A.G MEDICAL PRODUCTS AGRICULTURAL COOPERATIVE ASSOCIATION·10810190010966·

    Titanium Universal Abutment

    FDA UDI
    NOGA MEDICAL PRODUCTS LTD·07290118141457·Titanium Universal Abutment

    ARK Healing Cap 8mm PEEK

    FDA UDI
    NOGA MEDICAL PRODUCTS LTD·07290118142928·ARK Healing Cap 8mm PEEK

    BD¿ SYRINGE WITH NEEDLE

    FDA Adverse Event
    Malfunction ·BECTON DICKINSON·Product code FMI·November 9, 2018

    HYDROPHILIC COATED CATHETER

    FDA 510(k)
    FDA Class 1 ·Anesthesiology

    EVERFLEX SELF-EXPANDING PERIPHERAL STENT WITH ENTRUST DELIVERY SYSTEM LONG

    FDA Adverse Event
    Malfunction ·COVIDIEN·Product code NIP·March 9, 2016

    Stent, Superficial Femoral Artery

    FDA Pre-Market Approval
    FDA Class 3 ·EVERFLEX SELF-EXPANDING PERIPHERAL STENT SYSTEM (EVERFLEX)

    Implant, Hearing, Active, Middle Ear, Partially Implanted

    FDA Pre-Market Approval
    FDA Class 3 ·SOUNDTEC DIRECT SYSTEM

    EVERFLEX SELF-EXPANDING PERIPHERAL STENT WITH ENTRUST DELIVERY SYSTEM LONG

    FDA Adverse Event
    Malfunction ·COVIDIEN·Product code NIP·March 9, 2016

    NATURALYTE

    FDA Adverse Event
    Death ·FRESENIUS MEDICAL CARE NORTH AMERICA·Product code KPO·April 25, 2014

    530G INSULIN PUMP

    FDA Adverse Event
    Injury ·MEDTRONIC PUERTO RICO OPERATIONS CO.·Product code OZO·June 1, 2015

    ULTRAPRO MESH

    FDA Adverse Event
    Injury ·ETHICON, INC.·Product code FTL·August 12, 2010

    Stent, Superficial Femoral Artery

    FDA Pre-Market Approval
    FDA Class 3 ·EverFlex™ Self-Expanding Peripheral Stent with Entrust™ Delivery System

    Stent, Superficial Femoral Artery

    FDA Pre-Market Approval
    FDA Class 3 ·EVERFLEX SELF-EXPANDING PERIPHERAL STENT SYSTEM (EVERFLEX)

    Stent, Superficial Femoral Artery

    FDA Pre-Market Approval
    FDA Class 3 ·EverFlex Self-Expanding Peripheral Stent System, EverFlex Self-Expanding Peripheral Stent System with Entrust Delivery S

    Implant, Hearing, Active, Middle Ear, Partially Implanted

    FDA Pre-Market Approval
    FDA Class 3 ·MAXUM SYSTEM

    Stent, Superficial Femoral Artery

    FDA Pre-Market Approval
    FDA Class 3 ·EverFlex™ Self-Expanding Peripheral Stent System; EverFlex™ Self-Expanding Peripheral Stent with Entrust™ Delivery Syste

    Stent, Superficial Femoral Artery

    FDA Pre-Market Approval
    FDA Class 3 ·EVERFLEX SELF-EXPANDING PERIPHERAL STENT SYSTEM