Foshan Pingchuang Medical Technology Co., Ltd.

News & Events

Warmly celebrate our company's personal lubricant passed the certification of the Philippine Food and Drug Administration

Jun. 15, 2023

On February 15, 2022, Pingchuang Medical's human body lubricants officially passed the certification of the Philippine Food and Drug Administration! This marks that our company's personal lubricants can be successfully exported to the Philippines since then, and our foreign trade team has made another success in the Southeast Asian market.

team

Our company's human body lubricant export qualification system has been rapidly improved in recent years, and has passed ISO13485, EU CE certification, US FDA 510(K) certification, etc., and the export territory has also expanded accordingly, from Japan and South Korea to Europe and the United States at the beginning. Up to today's Southeast Asia, the number of export trading countries is on the rise. The reason why our company's export business has achieved such a rapid growth in recent years is inseparable from the dedicated research and development and production of colleagues in the company's production department, customers' recognition of our products and services, and the hard work of the foreign trade team.

Sterile Workshop

Seeing this, many friends who do export may be more confused: Do we need so many qualifications to export human lubricants? The answer is yes. In many countries, human body lubricants are actually medical device products rather than civilian products. Therefore, there are certain differences from domestic sales. No matter which country the medical device product is from, the qualification review is very strict. The long cycle and the difficulty of passing the review are its characteristics. Although the profit of the export trade of human body lubricants is very considerable, the difficulty of export qualification review is the reason why most companies shrink back.

Since its establishment, our company has been deeply involved in the field of gel medical devices. According to the GMP production management regulations, we have invested a lot of money to build a 100,000-level sterile medical device production workshop and a 10,000-level laboratory and inspection room. The product quality of human lubricants can prevent the qualification review from being blocked due to product quality defects. On the one hand, it can shorten the qualification review time, and on the other hand, it can also reduce the handover burden of export customers to the greatest extent. people's hearts.

Sterile Workshop