Data / Medical devices / Set, I.V. Fluid Transfer / China
FDA-registered makers of Set, I.V. Fluid Transfer in China: 7 establishments
7 establishments in China are registered with the FDA to make Set, I.V. Fluid Transfer (product code LHI). 4 have a 510(k) clearance or PMA approval on file and 0 have a recall event. FDA data exported November 2, 2026.
SpecStream is the live web data engine for teams and agents. It reads the FDA registration and listing, 510(k), PMA, recall and enforcement files from openFDA every week, and this page is that reading, joined by the FDA's own numbers. Ask for the makers of any device type in any country and new clearances, approvals and recalls arrive in your sheet, CRM, Slack or agent as the FDA publishes them.
- Device
- Set, I.V. Fluid Transfer
- Product code
- LHI
- Country
- China
Makers of Set, I.V. Fluid Transfer in China
| Maker | Location | Role | 510(k) clearances | Latest clearance | PMA approvals | Recall events | Class I | Source |
|---|---|---|---|---|---|---|---|---|
| Hangzhou Qiantang Longyue Biotechnology Co.,Ltd | Hangzhou Zhejiang, China | Manufacturer | 4 | June 5, 2026 | 0 | 0 | 0 | api.fda.gov |
| Gcmedica Enterprise Ltd. (wuxi) | Wuxi Jiangsu, China | Contract manufacturer, Manufacturer | 1 | December 2, 2019 | 0 | 0 | 0 | api.fda.gov |
| Gcmedica Enterprise Ltd.(wuxi) | WUXI Jiangsu, China | Manufacturer | 1 | December 2, 2019 | 0 | 0 | 0 | api.fda.gov |
| Zhejiang Medtec Medical devices Co., Ltd | Hangzhou Zhejiang, China | Manufacturer | 1 | July 11, 2012 | 0 | 0 | 0 | api.fda.gov |
| Gri Medical & Electronic Technology Co., Ltd. | JIAXING Zhejiang, China | Contract manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Ming Fai Industrial (shenzhen) Co. Ltd. | SHENZHEN Guangdong, China | Contract manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Suzhou Jinsheng Plastic Co., Ltd. | SUZHOU Jiangsu, China | Contract manufacturer | 0 | 0 | 0 | 0 | api.fda.gov |
Updated November 2, 2026. 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.