Data / Medical devices / China / Medstar Medical Int'l (shanghai) Co., Ltd.
Medstar Medical Int'l (shanghai) Co., Ltd.: FDA-registered device maker in Shanghai, China, 1 510(k) clearance
Medstar Medical Int'l (shanghai) Co., Ltd. is registered with the FDA (registration 3005695733) in Shanghai, China. It lists 1 device type. The FDA files 1 510(k) clearance under its listings, the newest dated May 15, 2015. Registered through 2026. FDA data exported November 3, 2026.
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- FDA registration number
- 3005695733
- Address
- Room 1123, Cimic Tower, 1090 Century Boulevard, Shanghai, China, 200122
- Owner or operator
- Medstar Medical Int'l (Shanghai) Co., Ltd. (10047998)
- Roles
- Exporter to the US
- First device listed
- October 23, 2017
- Registered through
- 2026
- Brand names listed
- blood pressure cuff
Devices it lists
| Device | Product code | Class | Role | Source |
|---|---|---|---|---|
| Blood Pressure Cuff | DXQ | 2 | Exporter to the US | accessdata.fda.gov |
510(k) clearances
The 510(k) numbers this establishment lists, with the FDA decision on each. The applicant is the company that holds the clearance.
| Decided | 510(k) number | Device | Product code | Decision | Applicant | Source |
|---|---|---|---|---|---|---|
| May 15, 2015 | K143728 | Minhua Disposable Blood Pressure Cuff | DXQ | Substantially Equivalent | Suzhou Minhua Medical Apparatus | accessdata.fda.gov |
Compare with other makers
Updated May 15, 2015. Read from openFDA bulk downloads (device registration and listing, 510(k), PMA, recall and enforcement files). CC0 1.0, public domain (openFDA terms of service). The files are joined on FDA identifiers: the 510(k) and PMA numbers a registration lists, and the recalling firm's FEI for recalls. Recall class comes from the FDA enforcement report. The FDA states that openFDA data is unvalidated and is not for decisions about medical care. Free to reuse with credit to SpecStream under CC BY 4.0. Spot a wrong value? Write to [email protected] with the link to this page.