Data / Medical devices / China / Beijing Demax Medical Technology Co., Ltd.
Beijing Demax Medical Technology Co., Ltd.: FDA-registered device maker in Beijing, China, 4 510(k) clearances
Beijing Demax Medical Technology Co., Ltd. is registered with the FDA (registration 3010141307) in Beijing, China. It lists 5 device types. The FDA files 4 510(k) clearances under its listings, the newest dated August 22, 2024. Registered through 2026. FDA data exported November 2, 2026.
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- FDA registration number
- 3010141307
- Address
- A13-7, Jingshengnansi Street, 101102 Beijing, P. R. China, Beijing, China, 101102
- Owner or operator
- BEIJING DEMAX MEDICAL TECHNOLOGY CO., LTD. (10048899)
- Roles
- Manufacturer
- First device listed
- March 17, 2015
- Registered through
- 2026
- Brand names listed
- Arm Support Board, Balloon In-deflation Device, DBQ05102120, DBQ05102120L, DBQ05102120LS, DBQ05102120LT, DBQ05102120S, DBQ05102120T and more
Devices it lists
| Device | Product code | Class | Role | Source |
|---|---|---|---|---|
| Adaptor, Stopcock, Manifold, Fitting, Cardiopulmonary Bypass | DTL | 2 | Manufacturer | accessdata.fda.gov |
| Board, Arm (With Cover), Non-Sterile | NOD | 1 | Manufacturer | accessdata.fda.gov |
| Clamp, Vascular | DXC | 2 | Manufacturer | accessdata.fda.gov |
| Introducer, Catheter | DYB | 2 | Manufacturer | accessdata.fda.gov |
| Syringe, Balloon Inflation | MAV | 2 | Manufacturer | 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 |
|---|---|---|---|---|---|---|
| August 22, 2024 | K242248 | Introducer Sheath Kits | DYB | Substantially Equivalent | Beijing Demax Medical Technology Co.,Ltd | accessdata.fda.gov |
| February 21, 2023 | K222184 | Introducer Sheath Kits | DYB | Substantially Equivalent | Beijing Demax Medical Technology Co.,Ltd | accessdata.fda.gov |
| January 4, 2023 | K222182 | Radial Artery Compression Tourniquets | DXC | Substantially Equivalent | Beijing Demax Medical Technology Co.,Ltd | accessdata.fda.gov |
| March 5, 2015 | K140943 | MASTRO PLUS BALLOON IN-DEFLATION DEVICE | MAV | Substantially Equivalent | Beijing Demax Medical Technology Co.,Ltd | accessdata.fda.gov |
Compare with other makers
- All makers of Clamp, Vascular
- All makers of Introducer, Catheter
- All makers of Adaptor, Stopcock, Manifold, Fitting, Cardiopulmonary Bypass
- All makers of Syringe, Balloon Inflation
- All makers of Board, Arm (With Cover), Non-Sterile
Updated August 22, 2024. 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.