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Klinische Studien
Import
Implementation MDR, IVDR
Distribution
CE mark
Medical device legislation is defined at European level within the framework of directives and regulations which are to be observed in full in the near future, and at national level within the framework of the Medical Devices Act as well as various more specific ordinances.
Tenders
Supply contracts
List of aids
Therapeutic appliances within the meaning of § 33 SGB V are all means required by the insured person to ensure the success of a medical treatment, to prevent an impending disability or to accommodate a disability. This includes hearing aids, orthopaedic insoles, electro stimulation devices, prostheses as well as software. As a rule, therapeutic appliances are reimbursed by the statutory health insurance funds based on a medical prescription.
Social
WHEN IT MATTERS.