BEUDAMED
    171 results · 19ms · Sources: EU EUDAMED, US FDA
    Filters Classification: FDA Class 2 ×

    SOLAR GI

    FDA 510(k)
    FDA Class 2 ·Gastroenterology, Urology

    Device For Home Collection And Transport Of Vaginal Specimens By Lay Users For Use In An Approved Hpv Molecular Assay

    FDA classification
    FDA Class 2 ·Device For Home Collection And Transport Of Vaginal Specimens By Lay Users For Use In An Approved Hpv Molecular Assay

    Intra-Pulmonary Percussive Vibration (Ipv) Devices

    FDA classification
    FDA Class 2 ·Intra-Pulmonary Percussive Vibration (Ipv) Devices

    Prosthesis, Knee, Patello/Femorotibial, Semi-Constrained, Uhmwpe, Pegged, Cemented, Polymer/Metal/Polymer

    FDA classification
    FDA Class 2 ·Prosthesis, Knee, Patello/Femorotibial, Semi-Constrained, Uhmwpe, Pegged, Cemented, Polymer/Metal/Polymer

    Syringe, Balloon Inflation

    FDA classification
    FDA Class 2 ·Syringe, Balloon Inflation

    Syringe, Balloon Inflation, Exempt

    FDA classification
    FDA Class 2 ·Syringe, Balloon Inflation, Exempt

    Catheters, Transluminal Coronary Angioplasty, Percutaneous

    FDA Pre-Market Approval
    FDA Class 2 ·PRIME{TM} MODEL 6520, 6525, 6530 AND 6535

    Catheters, Transluminal Coronary Angioplasty, Percutaneous

    FDA Pre-Market Approval
    FDA Class 2 ·PRIME{TM} MODEL 6520, 6525, 6530 AND 6535

    Catheters, Transluminal Coronary Angioplasty, Percutaneous

    FDA Pre-Market Approval
    FDA Class 2 ·PRIME{TM} MODEL 6520, 6525, 6530 AND 6535

    Catheters, Transluminal Coronary Angioplasty, Percutaneous

    FDA Pre-Market Approval
    FDA Class 2 ·PRIME{TM} MODEL 6520, 6525, 6530 AND 6535

    Catheters, Transluminal Coronary Angioplasty, Percutaneous

    FDA Pre-Market Approval
    FDA Class 2 ·PRIME{TM} MODEL 6520, 6525, 6530 AND 6535