BEUDAMED
    238 results · 26ms · Sources: EU EUDAMED, US FDA

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    Catheter, Coronary, Atherectomy

    FDA Pre-Market Approval
    FDA Class 3 ·IVT CORONARY ATHERECTOMY SYSTEM (TEC)(R)

    Catheter, Coronary, Atherectomy

    FDA Pre-Market Approval
    FDA Class 3 ·IVT CORONARY ATHERECTOMY SYSTEM (TEC)(R)

    Catheter, Coronary, Atherectomy

    FDA Pre-Market Approval
    FDA Class 3 ·IVT CORONARY ATHERECTOMY SYSTEM (TEC)(R)

    Catheter, Coronary, Atherectomy

    FDA Pre-Market Approval
    FDA Class 3 ·IVT CORONARY ATHERECTOMY SYSTEM (TEC)(R)

    Catheter, Coronary, Atherectomy

    FDA Pre-Market Approval
    FDA Class 3 ·IVT CORONARY ATHERECTOMY SYSTEM (TEC)(R)

    Catheter, Coronary, Atherectomy

    FDA Pre-Market Approval
    FDA Class 3 ·IVT CORONARY ATHERECTOMY SYSTEM (TEC)(R)

    DeRoyal

    FDA UDI
    DEROYAL INDUSTRIES, INC.·00749756978774·SCLERA PROCESSING KIT

    Multi-Unit H4mm

    FDA UDI
    T.A.G MEDICAL PRODUCTS AGRICULTURAL COOPERATIVE ASSOCIATION·10810190011635·

    Anatomic Healing Cap 6mm Wide

    FDA UDI
    T.A.G MEDICAL PRODUCTS AGRICULTURAL COOPERATIVE ASSOCIATION·10810190011475·

    Anatomic Healing Cap 6mm Wide

    FDA UDI
    NOGA MEDICAL PRODUCTS LTD·07290118142898·Anatomic Healing Cap 6mm Wide

    Multi-Unit H4mm

    FDA UDI
    NOGA MEDICAL PRODUCTS LTD·07290118143161·Multi-Unit H4mm

    NOVAMETRIX MODEL 1265 END TIDAL CARBON DIOXIDE MON

    FDA 510(k)
    FDA Class 2 ·Anesthesiology

    ENSEAL G2 ARTICULATING

    FDA Adverse Event
    Malfunction ·ETHICON ENDO-SURGERY, LLC.·Product code GEI·May 10, 2017

    CAPSULECLOSE SCORPION

    FDA Adverse Event
    Malfunction ·ARTHREX, INC.·Product code LXH·May 24, 2021

    CAPSULECLOSE SCORPION

    FDA Adverse Event
    Malfunction ·ARTHREX, INC.·Product code LXH·July 27, 2021

    SWEET PICOTIP

    FDA Adverse Event
    Injury ·CPI - DEL CARIBE·Product code NVN·January 11, 2013

    8800

    FDA Adverse Event
    Malfunction ·GE MEDICAL SYSTEMS (INDIA) PRIVATE LTD·Product code JAA·November 10, 2010

    ETS LINEAR CUTTER

    FDA Adverse Event
    Malfunction ·ETHICON ENDO-SURGERY, LLC.·Product code GDW·July 2, 2014

    Coronary Drug-Eluting Stent

    FDA Pre-Market Approval
    FDA Class 3 ·Xience Skypoint Everolimus Eluting Coronary Stent System

    Lenses, Soft Contact, Extended Wear

    FDA Pre-Market Approval
    FDA Class 3 ·FOCUS NIGHT AND DAY (LOTRAFILCON A) SOFT CONTACT LENSES