BEUDAMED
    10,000 results · 49ms · Sources: EU EUDAMED, US FDA

    21 CoolFlex

    FDA UDI
    SIGVARIS INC·00745129310370·Inelastic garment (or accessory) made of nylon ...

    21 CoolFlex

    FDA UDI
    SIGVARIS INC·00745129310301·Inelastic garment (or accessory) made of nylon ...

    21 CoolFlex

    FDA UDI
    SIGVARIS INC·00745129310462·Inelastic garment (or accessory) made of nylon ...

    System, Test, Her-2/Neu, Ihc

    FDA Pre-Market Approval
    FDA Class 3 ·PATHWAY ANTI-HER2/NEU (4B5) RABBIT MONOCLONAL PRIMARY ANTIBODY

    System, Test, Her-2/Neu, Ihc

    FDA Pre-Market Approval
    FDA Class 3 ·PATHWAY ANTI-HER-2/NEU (4B5) RABBIT MONOCLONAL PRIMARY ANTIBODY

    H3R-0039

    Basic UDI-DI
    EU MDR · Eu Md Class 2a ·TZ Medical inc·1 device

    Ankle harness

    Basic UDI-DI
    EU MDR · Eu Md Class 1 ·Medtex Swiss Ltd·1 device

    H3R-0040

    Basic UDI-DI
    EU MDR · Eu Md Class 2a ·TZ Medical inc·1 device

    Wrist harness

    Basic UDI-DI
    EU MDR · Eu Md Class 1 ·Medtex Swiss Ltd·1 device

    Pavlik harness

    Basic UDI-DI
    EU MDR · Eu Md Class 1 ·Medtex Swiss Ltd·3 devices

    Adjustable Harness

    Basic UDI-DI
    EU AIMDD · Eu Aimdd Class ·Aleva Neurotherapeutics SA·1 device

    EVO and PATHFINDER SL

    FDA UDI
    SPACELABS HEALTHCARE (WASHINGTON), INC·10841522127229·PACKAGE, EVO AND PATHFINDER SL

    CAPS

    FDA UDI
    VESTIBULAR TECHNOLOGIES, LLC·B702P31C0·Lightweight, portable, state of the art three-c...

    AI100 with Shonit

    FDA 510(k)
    FDA Class 2 ·Hematology

    Test, Fluorescence In Situ Hybridization (Fish), For Bladder Cancer Detection And Monitoring For Recurrence

    FDA Pre-Market Approval
    FDA Class 3 ·URO VYSION BLADDER CANCER KIT

    System, Test, Her-2/Neu, Nucleic Acid Or Serum

    FDA Pre-Market Approval
    FDA Class 3 ·THE PATH VYSION HER-2 DNA PRODE KIT

    Fluorescence In Situ Hybridization, Anaplastic Lymphoma Kinase, Gene Rearrangement

    FDA Pre-Market Approval
    FDA Class 3 ·VYSIS ALK BREAK APART FISH PROBE KIT

    Device, Thermal Ablation, Endometrial

    FDA Pre-Market Approval
    FDA Class 3 ·HER OPTION (TM) UTERINE CRYOBLATION THERAPY SYSTEM

    System, Test, Her-2/Neu, Nucleic Acid Or Serum

    FDA Pre-Market Approval
    FDA Class 3 ·Path Vysion HER-2 DNA Probe Kit

    System, Test, Her-2/Neu, Nucleic Acid Or Serum

    FDA Pre-Market Approval
    FDA Class 3 ·Path Vysion HER-2 DNA Probe Kit