BEUDAMED
    19 results · 41ms · Sources: EU EUDAMED, US FDA

    Hidroxa SE30

    FDA registration
    Hidroxa Medical AB·1 product·🇸🇪 Sweden

    Hidroxa SE30

    FDA 510(k)
    FDA Class 2 ·Physical Medicine

    Device, Iontophoresis, Other Uses

    FDA classification
    FDA Class 2 ·Device, Iontophoresis, Other Uses

    LCP

    FDA UDI
    Synthes GmbH·10886982166296·3.5MM LCP® POSTEROLATERAL DISTAL HUMERUS PLATE ...

    OsteoMed

    FDA UDI
    OSTEOMED LLC·00845694022897·FPS 2.7mm 5.0mm Wedge Plate

    VS Series Vital Signs Monitors (Including VS 9/VS 8/VS 8A)

    FDA registration
    SHENZHEN MINDRAY BIO-MEDICAL ELECTRONICS CO., LTD.·1 product·🇨🇳 China

    Adaptix Interbody System with Titan nanoLOCK Surface Technology

    FDA registration
    Sterigenics US, LLC·2 products·🇺🇸 United States

    VS Series Vital Signs Monitors (Including VS 9/VS 8/VS 8A)

    FDA registration
    Shenzhen Mindray Bio-Medical Electronics Co.,LTD·1 product·🇨🇳 China

    Vital Signs Monitors VS 8

    FDA registration
    MINDRAY DS USA, Inc.·1 product·🇺🇸 United States

    Adaptix™ Interbody System with Titan nanoLock™ Surface Technology

    FDA registration
    MEDTRONIC SOFAMOR DANEK USA, INC.·2 products·🇺🇸 United States

    Adaptix™ Interbody System with Titan nanoLock™ Surface Technology

    FDA registration
    Medtronic Engineering and Innovation Center (MEIC)·2 products·🇮🇳 India

    VS 8 Vital Signs Monitor, VS 8A Vital Signs Monitor, VS 9 Vital Signs Monitor

    FDA registration
    Flextronics Manufacturing (Singapore) Pte Ltd·1 product·🇸🇬 Singapore

    Adaptix™ Interbody System with Titan nanoLock™ Surface Technology

    FDA registration
    Titan Spine, a Division of Medtronic·2 products·🇺🇸 United States

    Thermalite Heated CPAP Tube

    FDA registration
    EXCELERON MEDICAL·2 products·🇺🇸 United States

    OsteoMed

    FDA UDI
    OSTEOMED LLC·00845694077361·FPS 2.7 5mm Wedge Plate Sterile Qty 2

    Adaptix Interbody System with Titan nanoLOCK Surface Technology

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    CARDIQ ANALYSIS III

    FDA 510(k)
    FDA Class 2 ·Radiology

    System, X-Ray, Tomography, Computed

    FDA classification
    FDA Class 2 ·System, X-Ray, Tomography, Computed

    Intervertebral Fusion Device With Bone Graft, Lumbar

    FDA classification
    FDA Class 2 ·Intervertebral Fusion Device With Bone Graft, Lumbar