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The CE mark is a necessary prerequisite for being able to sell a medical product on the German and European market - but not a sufficient prerequisite for (adequate) reimbursement of the service provider for the use of the medical product.

Adequate reimbursement for new examination and treatment methods based on the use of a medical device is, however, one of the decisive factors for the acceptance of the medical device on the market and is therefore essential for the manufacturer concerned.

German legislation provides for a number of ways in which reimbursement for new examination and treatment methods is established. With our technical expertise and experience, we can make a decisive contribution to the success of your company.


Operation and procedure code


Innovative examination and treatment methods


Evidence-based benefit assessment according to § 137h SGB V


Directory for outpatient billing


Trial procedure according to § 137e SGB V

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