BEUDAMED
    52 results · 47ms · Sources: EU EUDAMED, US FDA

    EchoGo Heart Failure (2)

    FDA registration
    ULTROMICS, LTD.·1 product·🇬🇧 United Kingdom

    EchoGo Heart Failure (2.0)

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    Adjunctive Heart Failure Status Indicator

    FDA classification
    FDA Class 2 ·Adjunctive Heart Failure Status Indicator

    NA

    FDA UDI
    Stryker Leibinger GmbH & Co. KG·07613327590968·STERNALPLATE, HEX, NARROW

    MEDI

    FDA UDI
    MEDI MANUFACTURING, INC.·00636257116630·30-40 MEDIVEN DUAL LAYER CALF BEIGE M

    SOPIX INSIDE, SOPIX2 INSIDE

    FDA registration
    SOPRO·1 product·🇫🇷 France

    X100HT with Full Field Peripheral Blood Smear (PBS) Application

    FDA registration
    SCOPIO LABS LTD.·1 product·🇮🇱 Israel

    COE TRAY PLASTIC™

    FDA UDI
    Gc America Inc.·10386040006354·COE TRAY PLASTIC™ Regular set-White powder 3 l...

    NA

    FDA UDI
    SYNTHES (U.S.A.) LP·10886982164346·4.5MM PROXIMAL TIBIA PLATE 12 HOLES/LEFT

    COE TRAY PLASTIC™

    FDA UDI
    Gc America Inc.·D6582400131·COE TRAY PLASTIC™ Regular set-White powder 3 l...

    Plateau-X Spacer System

    FDA UDI
    Life Spine, Inc.·00190837012472·

    Silk'n Titan AllWays

    FDA registration
    IBE Electronics Co., Ltd.·2 products·🇨🇳 China

    Titan Mini

    FDA registration
    SILKN CANADA CORP.·2 products·🇨🇦 Canada

    CORIOGRAPH Pre-Op Planning and Modeling Service

    FDA registration
    Smith & Nephew, Inc.·5 products·🇺🇸 United States

    Percutaneous Cardiac Ablation Catheter For Treatment Of Atrial Fibrillation With Irreversible Electroporation

    FDA Pre-Market Approval
    FDA Class 3 ·Sphere-9 Catheter and Affera Ablation System

    Percutaneous Cardiac Ablation Catheter For Treatment Of Atrial Fibrillation With Irreversible Electroporation

    FDA Pre-Market Approval
    FDA Class 3 ·Sphere-9 Catheter and Affera Ablation System

    SOPIX INSIDE, SOPIX2 INSIDE

    FDA 510(k)
    FDA Class 2 ·Dental

    ANGIOJET XPEEDIOR 120 CATHETER AND ANGIOJET POWER PULSE SPRAY ANCILLARY KIT

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    Kyocera Medical Technologies, Inc.

    FDA UDI
    KYOCERA MEDICAL TECHNOLOGIES, INC.·00841523132744·ACP, Ø4mm x 13mm, Variable Angle Screw, Self-Ta...

    HexaPulse™ PF Generator - AFR-00008

    FDA registration
    PLEXUS CORP.·3 products·🇺🇸 United States