This public data was collected to strengthen quality control and monitor the status of companies holding valid GMP (Good Manufacturing Practice) certifications by providing integrated information on the designation status of medical device manufacturers and importers. - It includes basic information such as company name, manufacturer, and address, as well as detailed items such as applicable standards, review status, certification number, certification validity period, and approval date. - Through this, it transparently discloses the status of manufacturing and import stability and regulatory compliance, and is expected to yield various benefits, including the analysis of the number and results of GMP-certified companies and the evaluation of the appropriateness of sales operations by manufacturers and importers.