As international regulations continue to evolve, compliance has become an essential part of supplying disposable hygiene products to global markets.

To better support customers in different regions, we continue to strengthen our quality management system and regulatory compliance across our manufacturing operations.

Our manufacturing facility operates under an ISO 13485 quality management system, supporting the production of disposable medical and hygiene products with standardized manufacturing procedures.

For customers serving the European market, our disposable underpads comply with the requirements of the EU Medical Device Regulation (EU) 2017/745 (MDR) for applicable products. We also maintain the necessary documentation to support regulatory requirements in relevant markets.

To better serve customers in the United States, our facility maintains FDA Establishment Registration and Device Listing for applicable products, supporting international business cooperation where required.

As a manufacturing partner, we understand that compliance is more than documentation. It represents our commitment to consistent manufacturing, product quality, and responsible cooperation with customers worldwide.

We will continue improving our quality management system and manufacturing capabilities to support distributors, importers, and healthcare brands with reliable disposable hygiene products.