Recently, MAXIM MEDICAL and LABWARE CO., LTD announced a significant achievement: successfully passing the dual certification review for ISO 14001 International Environmental Management System and ISO 13485 Medical Device Quality Management System. The certification covers all business segments, including production, R&D, and foreign trade, signifying that the company has met globally recognized standards in green production, quality control, and compliant operation, thus laying a solid foundation for further expansion into the global high-end medical market.

The successful completion of the ISO 14001 Environmental Management System certification is a high affirmation of MAXIM MEDICAL and LABWARE CO., LTD production philosophy and practices. For many years, the company has consistently adhered to the operating principle of "environmental protection first, sustainable development," comprehensively implementing green development concepts from production process optimization and equipment upgrades to waste treatment. Through the widespread adoption of environmentally friendly hot-dip galvanizing production lines, controlled atmosphere annealing furnaces, and other environmentally friendly equipment, as well as the application of automated energy-saving feeding systems, the company has reduced its unit product energy consumption by 30% compared to the industry average, significantly decreasing carbon emissions and forming a "highly efficient and environmentally friendly" green production model.

The successful review of the ISO 13485 medical device quality management system further demonstrates MAXIM MEDICAL and LABWARE CO., LTD stringent pursuit of product quality. The company has established a comprehensive compliance management system, rigorously selecting environmentally friendly medical-grade raw materials that meet international medical standards and establishing a robust raw material traceability mechanism. On the production side, it relies on a fully automated equipment cluster to achieve standardized and precise control of the production process. On the quality control side, it has established a professional compliance testing laboratory equipped with cutting-edge testing equipment, developing personalized testing solutions for different countries and regions' market access standards to ensure stable and controllable product quality.

The successful implementation of this dual certification not only enhances MAXIM MEDICAL and LABWARE CO., LTD credibility and competitiveness in the international market but also opens a green channel for its products to enter high-end medical markets such as the EU and North America. Currently, the company's core products have successfully entered medical institutions and research laboratories in Germany, France, the United States, and other countries and regions, leveraging the advantages of dual certification. "Compliance is the foundation of foreign trade enterprises, and green development is the core of sustainable development," said the company's compliance manager. He added that the company will continue to track global regulatory updates, continuously optimize its compliance management system, and build a globally trusted medical consumables brand based on the dual certification.