Shenzhen Mindray Bio-Medical Electronics Co., Ltd. (迈瑞医疗)
Company Overview
Shenzhen Mindray Bio-Medical Electronics Co., Ltd. (深圳迈瑞生物医疗电子股份有限公司) develops, manufactures and markets medical devices and solutions. The company was founded in 1991 and is headquartered in Shenzhen, China, with subsidiaries and branch offices across North and Latin America, Africa, Europe and Asia-Pacific. It is listed on the Shenzhen Stock Exchange under ticker 300760.
Mindray is one of the larger medical equipment companies in the world and a direct competitor to established Western and Japanese manufacturers in several of its product lines.
Main Products
The portfolio spans three broad areas of hospital and clinical equipment:
- Patient monitoring and life support: patient monitors, ventilators, defibrillators and AEDs, electrocardiographs, anaesthesia machines, and infusion systems.
- Medical imaging: ultrasound systems, radiology equipment and related accessories, including emergency and critical care ultrasound configurations.
- In-vitro diagnostics (IVD): chemistry, haematology, coagulation, urine and microbiology analysers, and chemiluminescence immunoassay (CLIA) systems.
Beyond hardware, the company supplies connected-care software and workflow solutions — for example ICU, OR, ER and CCU integration platforms — along with operating tables, surgical lights, medical supply units and animal medical products. It also offers OEM products.
Key Facts
- Founded: 1991.
- Headquarters: Mindray Building, Keji 12th Road South, High-Tech Industrial Park, Nanshan, Shenzhen, Guangdong, China.
- Listing: Shenzhen Stock Exchange, ticker 300760.
- Scale: approximately 21,000 employees, with reported revenue in the region of USD 4.6 billion for 2024.
- Chairman: Li Xiting; President: Wu Hao.
- Markets: hospitals, clinics and healthcare facilities worldwide, served through a direct and distributor network.
Why a Buyer Would Look at Them
Mindray is relevant to distributors, hospital groups and healthcare procurement teams looking for medical equipment outside the traditional Western brands, and increasingly to buyers in emerging markets where its price-to-performance ratio is attractive. For importers of medical devices, note that regulatory approval is market-specific and product-specific — clearance such as FDA 510(k), EU MDR CE marking, or local registration must be verified for each device and each market before purchase, and should be confirmed directly with the manufacturer.
Contact
For current regional offices, distributor enquiries and product documentation, refer to the official website at www.mindray.com. Regulatory certificates and product approvals should be verified with the manufacturer and the relevant authority, as this entry summarises publicly available information only.