Manufacturer and brand owner in Shanghai, China. 1 device type, 1 product catalogued, 3 clearances.
Shanghai Microport Medical (Group) Co., Ltd. is a specification developer holding a current FDA establishment registration. The registration covers Catheters, Transluminal Coronary Angioplasty, Percutaneous. 1 of its products is catalogued under its own name. Its earliest product listing with the FDA dates from 2023.
Registration
FDA registration record for Shanghai Microport Medical (Group) Co., Ltd. | Registered name | SHANGHAI MICROPORT MEDICAL (GROUP) CO., LTD |
| Status | Registered |
| Registration expires | 2026 |
| Registration number | 3034695832 |
| FEI number | 3034695832 |
| DUNS | 544811078 |
| Establishment type | Specification developer, Manufacturer |
Chinese Registration
Chinese company register details for Shanghai Microport Medical (Group) Co., Ltd. | Chinese legal name | 上海微创医疗器械(集团)有限公司 |
| Unified social credit code | 91310000607389788T |
| Source | NMPA UDI database |
Location
Address of Shanghai Microport Medical (Group) Co., Ltd. | City | Shanghai |
| Province | Shanghai |
| Address | 1661 Zhangdong Road, ZJ Hi-Tech Park |
| Postal code | 201203 |
| Country | China |
From the Company
Published by the company on its own website, not by the FDA.
Information published by Shanghai Microport Medical (Group) Co., Ltd. | Founded | 1998 |
| Main products | coronary stents, surgical robots, valve systems, flow diverter stents, orthopedic devices |
| Certifications | Hong Kong Stock Exchange (00853.HK) |
| Export markets | 100+ countries |
| OEM and ODM | Not offered |
Source: U.S. FDA establishment registration and device listing records, public domain. Restructured for clarity and searchability. Not affiliated with or endorsed by the FDA. Records are records: nothing here is an offer of sale.