Receiving a CE mark on a medical device is an enormous accomplishment for the manufacturer. A CE-mark allows the manufacturers to sell their medical device within the European Union (EU) and other countries that recognize the mark.
Unfortunately the CE mark alone is not enough. A strong and consistent demand for a medical device relies on reimbursement, and navigating the many regulations and applications for reimbursement approval can be tricky.
Formal reimbursement for the medical device is the foundation of sales.
Factory Reimbursement for Medical Devices is here to help you navigate through your reimbursement challenges and offers a tailor-made solution for all levels of Reimbursement issues in Europe.
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