This is the supplier profile page of HANGZHOU FUSHAN MEDICAL APPLIANCES CO ., LTD, where buyers can explore products, connect directly with the supplier for pricing inquiries.

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1.1

No1288 Jinxi South Street, Linan City

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Business Description

Fushan is a high-tech group of enterprises professional in medical area and devoted itself to researching, exploiting and manufacturing medical products of anaesthesiology, respiration, urology, gastroenterology, and wound drainage system. The headquarter of Fushan group is located in west suburb of Hangzhou City, which is the most beautiful city in China. Fushan, as a manufacturer of medical appliances with top international manufacturing technics and conditions, was newly designed and constructed totally in accordance with GMP standards and requirements. It is equipped with standard purification workshops of class 100, 000 , a large Ethylene Oxide Sterilization Cabinet, Physical and Chemical Testing Centers, imported advanced liquid-injection molding machine system from France and other excellent facilities. With the principle of “Standard, Scrupulous, Concentration, Creation”, Fushan provides excellent-quality products and sincere services, committing to caring human health in the world. We manage the company quality control system strictly according *****

Business Overview

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≤ 1h

HANGZHOU FUSHAN MEDICAL APPLIANCES CO., LTD. offers a specific medical product — drainage devices — which are in high demand in healthcare markets across Asia and Europe. Being founded in 2005 shows the company has years of experience in manufacturing and likely understands regulatory and quality expectations. However, the lack of verified work email, phone number, and business documents raises concerns about legitimacy and responsiveness. Buyers should request additional verification before placing large orders or sharing sensitive medical requirements. Without a verified contact, communication may be slow or unreliable. The origin in China provides access to cost-effective production, but buyers must confirm compliance with international medical device standards. A verified profile would help build trust and reduce risk in a regulated industry.

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