BEUDAMED
    10,000 results · 43ms · Sources: EU EUDAMED, US FDA

    JEIL BONE FIXATION SYSTEM

    FDA registration
    JEIL MEDICAL CORPORATION·2 products·🇰🇷 South Korea

    AGNES+

    FDA registration
    AGNES MEDICAL CO.,LTD·1 product·🇰🇷 South Korea

    ARIX Hand System

    FDA registration
    JEIL MEDICAL CORPORATION·2 products·🇰🇷 South Korea

    SO-35L-SO-L20-T

    FDA registration
    JEIL MEDICAL CORPORATION·2 products·🇰🇷 South Korea

    PALLAS Premium

    FDA registration
    LASEROPTEK·1 product·🇰🇷 South Korea

    Hi-dop

    FDA registration
    Bistos co., ltd.·1 product·🇰🇷 South Korea

    HYPERION Long Pulsed Nd:YAG Dermatological Laser

    FDA registration
    LASEROPTEK·1 product·🇰🇷 South Korea

    ARIX Ankle Fibula Hook Plate System

    FDA registration
    JEIL MEDICAL CORPORATION·1 product·🇰🇷 South Korea

    System, Appendage Closure, Left Atrial

    FDA Pre-Market Approval
    FDA Class 3 ·WATCHMAN FLX Pro Left Atrial Appendage Closure (LAAC) Device with Delivery System

    Device, Hemostasis, Vascular

    FDA Pre-Market Approval
    FDA Class 3 ·DIAGNOSTIC DUETT AND DUETT PRO SEALING DEVICES AND D-STAT FLOWABLE HEMOSTAT

    Sensor, Glucose, Invasive

    FDA Pre-Market Approval
    FDA Class 3 ·MEDTRONIC MINIMED CONTINUOUS GLUCOSE MONITORING SYSTEM: CARELINK PRO, MMT-7335 VERSION 3.0B

    Test, Urea Adult And Pediatric (Breath),

    FDA Pre-Market Approval
    FDA Class 3 ·PyloPlus Urea Breath Test Pro Analyzer, PyloPlus Urea Breath Test Lab Analyzer

    System, Appendage Closure, Left Atrial

    FDA Pre-Market Approval
    FDA Class 3 ·WATCHMAN FLX Pro Left Atrial Appendage Closure (LAAC) Device with Delivery System

    Filler, Bone Void, Non-Osteoinduction

    FDA Pre-Market Approval
    FDA Class 3 ·PRO OSTEON IMPLANT 500 CORALLINE HYDROXYPATITE BONE VOID FILLER (FORMERLY INTERPORE 500)

    Filler, Bone Void, Non-Osteoinduction

    FDA Pre-Market Approval
    FDA Class 3 ·PRO OSTEON IMPLANT 500 CORALLINE HYDROXYPATITE BONE VOID FILLER (FORMERLY INTERPORE 500)

    Aid, Surgical, Viscoelastic

    FDA Pre-Market Approval
    FDA Class 3 ·Sodium Hyaluronate Ophthalmic Viscoelastic Device (OVD), Healon Duet® PRO Dual Pack

    System, Appendage Closure, Left Atrial

    FDA Pre-Market Approval
    FDA Class 3 ·WATCHMAN FLX™ Pro Left Atrial Appendage Closure (LAAC) Device with Delivery System

    Catheter, Percutaneous, Cardiac Ablation, For Treatment Of Atrial Fibrillation

    FDA Pre-Market Approval
    FDA Class 3 ·Arctic Front Advance®, Arctic Front Advance Pro® Cardiac CryoAblation Catheters

    Stent, Carotid

    FDA Pre-Market Approval
    FDA Class 3 ·CORDIS PRECISE NITINOL & RX NITINOL & PRO RX NITINOL STENT SYSTEM

    Pulse Generator, Permanent, Implantable

    FDA Pre-Market Approval
    FDA Class 3 ·DIVA PLATFORM IMPLANTABLE PULSE GENERATORS AND PRO VIT APPLICATION SOFTWARE VERSION 3.3.2