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Reimbursement summary for angioplasty of arteries of lower extremities

This post presents an extract from our reimbursement analysis for angioplasty of arteries lower extremities using plain and drug-coated balloons (DCBs) for peripheral artery disease in England, France and Germany. Plain balloon angioplasty is reimbursement via DRG solely and DCBs are reimbursement via combination of DRG and add-on reimbursement.
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The French National Authority for Health (HAS) published new set of decisions regarding add-on reimbursement of medical devices and medical aids in first half of November

The French National Authority for Health (HAS) published a new set of decisions in relation to add-on reimbursement of medical devices and reimbursement of medical aids that had been released by National Commission for Evaluation of Medical Devices and Health Technologies (CNEDiMTS) in the first half of November:

  • Five decisions were released for orthopedics devices:
    • TWIN CUP CEMENTED, double-mobility acetabular cup (application for registration, rejected due to insufficient expected benefit (AS))
    • XLMOB CEMENTED, double-mobility cemented cup (application for registration, rejected due to insufficient expected benefit (AS))
    • XLMOB NON CIMENTED, double-mobility non-cemented cup (application for registration, rejected due to insufficient expected benefit (AS))
    • SATURNE II (without cement), double-mobility non-cemented cup (application for registration, approved)
    • AIR,  meniscal repair system (application for registration, approved)
  • Two decisions were published for drug-coated balloons for peripheral vascular disease:
    • LUTONIX 035,  drug-coated balloon (application for registration, approved)
    • RANGER,   drug-coated balloon (application for registration, approved)
  • Two decisions concern devices for radiofrequency ablation procedure:
  • Four decisions consider other devices:
    • LIFECHOICE ACTIVOX 4L, portable oxygen concentrator (application for registration, approved)
    • URGO K2, two-layer bandage system for venous compression (request for renewal of registration, approved)
    • URGO K2 Latex Free, two-layer bandage system for venous compression (request for renewal of registration, approved)
    • ALLEVYN GENTLE BORDER HEEL, hydrocellular dressings (anatomical shape heel) (application for registration, approved)

See list of decisions in French here.

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