Whether buying or selling a medical device on the resale market, shipping can be a costly and problematic endeavour. This has created a corresponding increase in the number of medical devices being bought and sold on the "resale market". The FDA is responsible for protecting public health by ensuring the safety and efficacy of human and veterinary drugs, vaccines and other biological products, medical devices, food products, cosmetics, dietary supplements, tobacco products, and products that emit radiation. Please note that the basis of your supply business will be close cooperation with distributors and vendors of medical products.
The marketing of drugs and medical devices without CE marking is not prohibited in the US as long as applicable FDA requirements are met. Salinas, and are charged with conspiracy to steal prescription-only medical products and possession of the same stolen medical products. Ramey and Aderhold failed to instruct purchasers on the safe use of the stolen medical products. Another important aspect of the sale of medical equipment is the box or shipping container in which the original device was delivered.
Examples of medical devices include surgical instruments, implantable devices, diagnostic equipment, clinical laboratory tests and radiation-emitting medical products (e.g. products from the pharmaceutical industry). Approval from the FDA's Center for Devices and Radiological Health (CDRH) is required to export any type of medical device to the United States. The FDA is the primary agency with authority over the labelling, promotion and advertising of medical devices.
The FTC is responsible for regulating the advertising of many medical devices under sections 12-15 of the FTC Act, which prohibit false or misleading advertising of certain products regulated by the FDA.3 And in Canada, charities accept medical equipment, whether hospital beds, mattresses, furniture, wheelchairs, walkers or other devices. Federal legislation requires manufacturers and sellers of medical devices to follow numerous rules related to the approval and registration of devices, as well as how those products are labelled and marketed to consumers.