"MOH Registration Certificate"This may refer to a medical device registration certificate issued by a national health department. In general, the registration certificate of a medical device is one of the documents necessary to import and sell the product. This certificate indicates that the medical device has been reviewed by the health authorities and complies with the relevant regulations and standards for sale and use in the country.
In many countries, manufacturers or traders of medical devices need to obtain a certificate of registration from the health authorities of the target country before they can introduce their products to the market. This registration process may involve the submission of product information, quality control system documents, clinical trial data, etc. The issuance of registration certificates is often subject to compliance with the specific regulations and standards of the target country.
Therefore, if you plan to sell medical devices in a certain country, you will usually need to obtain a certificate of registration issued by the country's health department. Be sure to check the relevant regulations in your target country and follow the regulations of the country's health authorities. If you have a specific country or region issue, it is advisable to consult your local health department or professional legal counsel directly for accurate and up-to-date information.