#SFHS2612949ADelisting of the PROTEOR HYBRID-1P360 Prosthetic Knee from the Reimbursable Products List
AI-generated summary for informational purposes only. Not legal advice. See the original source for the authoritative text.
This order removes one PROTEOR prosthetic knee product, the HYBRID-1P360 mono-axial knee, from France’s reimbursable medical products and services list. The change mainly affects healthcare providers, prosthetics suppliers, patients using or considering this product, and reimbursement teams. From the effective date, the listed product code will no longer be covered under this entry, so procurement, prescribing, billing, and patient reimbursement checks should be updated.
AI-generated summary. May contain errors. Refer to official sources for legal decisions.
Key Changes
- Removes product code 2793482 for the PROTEOR HYBRID-1P360 mono-axial prosthetic knee from the reimbursable products list
- Applies to Title II, Section II, Chapter 3, optional variants for endoskeletal prostheses
- Takes effect on the thirteenth day after publication in the French Official Journal
Obligations
What this law requires
Remove LPPR code 2793482 for the PROTEOR HYBRID-1P360 mono-axial prosthetic knee from reimbursement, prescribing, procurement, billing, and coverage eligibility systems under Title II of the reimbursable products and services list.