We have a product that is used regularly patients that we needed to Nappi code and submit to various hospital groups. However, a requirement is that the item requires approval for funding from the medical aids. How do we go about applying for this funding approval for our medical product and who to contact at the different medical aids?

Related Knowledge Base Posts

• Does South Africa recognizes certification of medical devices approved in Australia?
• There is a local arm of a multinational that wants to know if their European principal’s QMS covers them or if they would need their own QMS as a subsidiary of the multinational. I enquired if they are subject to the principal’s QMS and they indicated that they are not as they are only the importer and do not manufacture locally but the international principal holds the ISAO13485 accreditation across its entire range of products (which makes sense because the company is ISO accredited and not the products themselves). Does the local subsidiary need to be listed on the international principal’s ISO accreditation or have its own?
• What are the ISO 13485 and conformity assessment bodies criteria for licence renewal?
• Are IVDs regulated in Mozambique?
• Who must I contact at SAHPRA if I have port health issues?
• Who must I contact at SAHPRA to report an adverse event?
• Who must I contact at SAHPRA to report poor quality or counterfeit medical devices?
• Who must I contact at SAHPRA regarding new licence applications
• Does SAHPRA allow re-sterilisation of a medical device?
• Is registration for medical devices required in Cameroon and what it would entail for registering of a medical device in this country?