Quality Products
Quality first is everything we do. As a legal manufacturer of sterile medical devices we are required to comply with the requirements of the FDA’s 21CFR 820, as well as ISO 13485. These specialized medical quality standards are the foundation of our quality management system and services. In addition, these stringent regulatory requirements ensure defect prevention, continuous improvement, reduction of waste and variation in the supply chain, and finally help us to deliver state-of-the-art products that meet or exceed the requirements.

Innovative Management
PROMED owes its success to the strong leadership and competence of the senior management team. With decades of broad experiences in medical product development and manufacturing cycles, the lead management team has assured continual success for the past and the future of PROMED. Meanwhile, we value our respectful and supportive teammates. We give our teammates clear direction with trust while encouraging their balanced lifestyle and individual development.

Cost Effective
Manufacture of sterile medical devices requires careful planning and allocation of resources in order to safeguard excellent performance. Meanwhile, it requires flexible and active collaboration throughout the organization so that product characteristics and manufacture competencies are in best combination without sacrificing product quality. The PROMED team truly partners and contributes his expertise to achieve our success in global medical market.

Environmentally Friendly
We think sustainably! We are committed to giving back to the society and environment. Long-term engagement is one of our strategic priorities. Non-hazardous materials complying REACH & RoHS directives are utilized in PROMED products. Meanwhile, we request similar support and cooperation from the entire supply chain from materials, critical components, assemblies and services providers.

Precise Surgery Disposable MicroFin Pencil and Electrode Datasheet