BEUDAMED
    53 results · 21ms · Sources: EU EUDAMED, US FDA

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    GEN4 DIGITAL

    FDA UDI
    CURBELL MEDICAL PRODUCTS, INC.·00840828132848·GEN4 DIGITAL

    Sensor, Electro-Optical (For Cervical Cancer)

    FDA Pre-Market Approval
    FDA Class 3 ·LUMA CERVICAL IMAGING SYSTEM

    Sensor, Electro-Optical (For Cervical Cancer)

    FDA Pre-Market Approval
    FDA Class 3 ·LUMA CERVICAL IMAGING SYSTEM

    Sensor, Electro-Optical (For Cervical Cancer)

    FDA Pre-Market Approval
    FDA Class 3 ·CERVICAL IMAGING SYSTEM

    Sensor, Electro-Optical (For Cervical Cancer)

    FDA Pre-Market Approval
    FDA Class 3 ·LUMA CERVICAL IMAGING SYSTEM

    Sensor, Electro-Optical (For Cervical Cancer)

    FDA Pre-Market Approval
    FDA Class 3 ·LUMA CERVICAL IMAGING SYSTEM

    GEN4 DIGITAL

    FDA UDI
    CURBELL MEDICAL PRODUCTS, INC.·00840828111287·GEN4 DIGITAL

    GEN4 Direct Access

    FDA UDI
    CURBELL MEDICAL PRODUCTS, INC.·00840828133562·GEN4 Direct Access

    GEN4 DIGITAL

    FDA UDI
    CURBELL MEDICAL PRODUCTS, INC.·00840828109406·GEN4 DIGITAL

    GEN4 DIGITAL

    FDA UDI
    CURBELL MEDICAL PRODUCTS, INC.·00840828111027·GEN4 DIGITAL

    GEN4 DIGITAL

    FDA UDI
    CURBELL MEDICAL PRODUCTS, INC.·00840828111256·GEN4 DIGITAL

    GEN4 DIRECT ACCESS

    FDA UDI
    CURBELL MEDICAL PRODUCTS, INC.·00840828147446·GEN4 DIRECT ACCESS

    GEN4 DIRECT ACCESS

    FDA UDI
    CURBELL MEDICAL PRODUCTS, INC.·00840828101332·GEN4 Direct Access

    GEN4 Direct Access

    FDA UDI
    CURBELL MEDICAL PRODUCTS, INC.·00840828105989·GEN4 Direct Access

    GEN4 DIRECT ACCESS

    FDA UDI
    CURBELL MEDICAL PRODUCTS, INC.·00840828111232·GEN4 DIRECT ACCESS

    GEN4 Direct Access

    FDA UDI
    CURBELL MEDICAL PRODUCTS, INC.·00840828101349·GEN4 Direct Access

    Intelliguides

    FDA UDI
    Mios Marketing, LLC·G2710410400280·Anterior Closing Wedge Osteotomy Guide, 40mm x ...

    Intelliguides

    FDA UDI
    Mios Marketing, LLC·G2710400400280·Anterior Dome Osteotomy Guide, 40mm x 28mm

    Intelliguides

    FDA UDI
    Mios Marketing, LLC·G2710420400280·Anterio Lateral Closing Wedge Osteotomy Guide, ...

    Intervertebral Fusion Device With Bone Graft, Lumbar

    FDA Pre-Market Approval
    FDA Class 2 ·AFFINITY (TM) CAGE SYSTEM