MAXIM MEDICAL and LABWARE CO., LTD. practices green and compliant production, meeting new global market access requirements with its core strengths.
Time : 2024-08-09

With the deepening of global "dual carbon" goals and the continuous improvement of quality and environmental protection requirements for medical devices in various countries, green compliance has become an essential condition for medical device foreign trade enterprises to participate in global competition. MAXIM MEDICAL and LABWARE CO., LTD. , based in the field of medical consumables foreign trade, promotes green production through technological upgrades and strengthens compliance management through standards. With the green quality and comprehensive compliance certification of its core products such as blood collection tubes, mini blood collection tubes, and microscope slides, it has successfully met the new requirements for global market access and won widespread market recognition and brand reputation in the international market.


Technological innovation is the core driving force of green production. To achieve green and environmentally friendly production processes, MAXIM MEDICAL and LABWARE CO., LTD has introduced internationally advanced environmentally friendly production equipment and processes, building an automated, green, and intelligent production system. Two environmentally friendly hot-dip galvanizing production lines enable environmentally friendly upgrades to the surface treatment process of medical consumables, eliminating toxic and harmful additives in traditional processes, ensuring product safety while achieving a green and pollution-free production process. The precise temperature control and energy-saving design of the controlled atmosphere annealing furnace significantly improves the energy utilization efficiency of the production process, helping the company achieve its development goals of energy conservation and emission reduction. Furthermore, the company's fully automated production equipment ensures a product yield rate of over 99%, and precise manufacturing processes guarantee that products fully meet international requirements for the size and precision of medical consumables, laying a solid foundation for quality as products enter the global market.


Compliance is the foundation of any foreign trade enterprise. MAXIM MEDICAL and LABWARE CO., LTD deeply understands the differences in medical device access rules across global markets and has established a comprehensive compliance management system to ensure barrier-free product export. On one hand, the company strictly adheres to the ISO 13485 international medical device quality management system requirements, standardizing the entire production process. From raw material inspection and production process control to finished product inspection, each step has clear operating standards and testing procedures, ensuring stable and controllable product quality. On the other hand, the company proactively completes international authoritative certifications for different target markets, covering EU CE, US FDA, and Canadian MDL certifications, allowing products to enter corresponding markets smoothly without additional testing, significantly shortening the market access cycle. Simultaneously, the company's compliance team closely monitors updates to medical device regulations in various countries, adjusting product production and certification strategies in a timely manner to ensure the company always stays at the forefront of compliant development.


MAXIM MEDICAL and LABWARE CO., LTD and compliant production philosophy has enabled its products to stand out in the global market. Currently, the company's blood collection tubes and mini blood collection tubes are exported to more than 50 countries and regions worldwide, becoming a preferred supplier for many overseas medical institutions and research laboratories. In the European market, the company's green production processes and the environmentally friendly attributes of its products meet the stringent requirements of the EU's Medical Device Regulation (MDR), resulting in year-on-year sales growth. In the North American market, thanks to FDA certification and high-standard product quality, the company has successfully penetrated the local mid-to-high-end medical consumables market.


A representative from MAXIM MEDICAL and LABWARE CO., LTD stated that green compliance is a strategic choice for the company's long-term development and a core advantage for participating in global healthcare industry competition. In the future, the company will continue to increase investment in green production technologies and compliance system construction, continuously optimize its product structure, enhance the green attributes and compliance of its products, and cultivate the global medical consumables market with higher-quality products and more professional services, contributing the strength of Chinese enterprises to promoting the green and compliant development of the global healthcare industry.


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