Global Cross-border Trade Business of Medical Devices and Consumables

Business Scope and Service Details

Relying on the Group's global platform and mature pharmaceutical trade system, the company expands two-way global cross-border trade of medical devices, medical consumables, in vitro diagnostic reagents, rehabilitation care and public health anti-epidemic materials. The core covered categories and services include:

1. Full Category Product Matrix: Medical consumables (infusion sets, syringes, indwelling needles, medical gloves, medical dressings, anti-epidemic materials), diagnosis and treatment equipment (infusion pumps, monitors, medical refrigeration equipment, operating room supporting equipment), in vitro diagnostic reagents (biochemical reagents, rapid test reagents), rehabilitation care and public health supporting equipment and other full category of medical products.

2. Full-process Supporting Services: Provide one-stop services including international certification docking such as CE/FDA/ISO 13485, product registration in target markets, global supply chain resource integration, OEM/ODM customized production, international logistics and customs clearance, product technical training and after-sales maintenance.

Core Support: Group's Industrial Advantages

1. Reuse Advantage of Global Brand and Channel Network: We share the Group's mature distributor network, hospital terminal resources and government cooperation channels covering more than 100 countries and regions around the world. Medical devices and consumables can quickly enter core markets such as Africa, Southeast Asia, the Middle East and the CIS, greatly reducing market expansion costs and access thresholds.

2. Extension of Pharmaceutical-grade Strict Quality Control System: We fully adopt the Group's pharmaceutical-grade GMP quality management system, implement strict qualification audit, incoming sampling inspection and full-process quality traceability for medical device and consumable suppliers, to ensure that all products are safe, compliant and stable in quality, far exceeding the general industry standards.

3. Mature International Compliance and Risk Control System: We are deeply familiar with the world's mainstream medical device regulations such as EU MDR, ISO 13485 and FDA QSR, and can provide full-process professional support including product classification definition, registration path planning, technical document (TDF) preparation, and label compliance audit, to help customers avoid compliance risks in cross-border trade.

Global Customer Value

Global hospitals, clinics, disease control institutions and medical device distributors can obtain: medical devices and consumables with pharmaceutical-grade quality control standards, one-stop compliance services for international registration and certification, rapid landing support through mature global channels, stable and controllable supply chain guarantee, and cost-effective full-category procurement solutions.