Data / Medical devices / Monitor, Physiological, Patient (Without Arrhythmia Detection Or Alarms) / China
FDA-registered makers of Monitor, Physiological, Patient (Without Arrhythmia Detection Or Alarms) in China: 16 establishments
16 establishments in China are registered with the FDA to make Monitor, Physiological, Patient (Without Arrhythmia Detection Or Alarms) (product code MWI). 10 have a 510(k) clearance or PMA approval on file and 0 have a recall event. FDA data exported November 2, 2026.
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- Device
- Monitor, Physiological, Patient (Without Arrhythmia Detection Or Alarms)
- Product code
- MWI
- Country
- China
Makers of Monitor, Physiological, Patient (Without Arrhythmia Detection Or Alarms) in China
| Maker | Location | Role | 510(k) clearances | Latest clearance | PMA approvals | Recall events | Class I | Source |
|---|---|---|---|---|---|---|---|---|
| Shenzhen Mindray Bio-Medical Electronics Co., Ltd. | Shenzhen Guangdong, China | Manufacturer | 7 | December 15, 2022 | 0 | 0 | 0 | api.fda.gov |
| Shenzhen Mindray Bio-Medical Electronics Co.,LTD | SHENZHEN Guangdong, China | Exporter to the US, Specification developer | 7 | December 15, 2022 | 0 | 0 | 0 | api.fda.gov |
| Guangdong Biolight Meditech Co., Ltd | Zhuhai Guangdong, China | Manufacturer | 5 | April 5, 2019 | 0 | 0 | 0 | api.fda.gov |
| Edan Instruments, Inc. | Shenzhen Guangdong, China | Manufacturer | 2 | March 8, 2024 | 0 | 0 | 0 | api.fda.gov |
| Shenzhen Creative Industry Co., Ltd | SHENZHEN Guangdong, China | Manufacturer | 2 | September 9, 2017 | 0 | 0 | 0 | api.fda.gov |
| Beijing Choice Electronic Technololgy Co., Ltd. | Beijing, China | Exporter to the US, Manufacturer | 1 | November 15, 2021 | 0 | 0 | 0 | api.fda.gov |
| Contec Medical Systems Co., Ltd | Qinhuangdao Hebei, China | Manufacturer | 1 | June 11, 2010 | 0 | 0 | 0 | api.fda.gov |
| Ge Medical Systems (china) Co., Ltd. | WUXI Jiangsu, China | Manufacturer | 1 | April 25, 2024 | 0 | 0 | 0 | api.fda.gov |
| Shenzhen Comen Medical Instruments Co., Ltd. | Shenzhen Guangdong, China | Contract manufacturer, Manufacturer | 1 | November 7, 2012 | 0 | 0 | 0 | api.fda.gov |
| Shenzhen Viatom Technology Co., Ltd. | Shenzhen Guangdong, China | Manufacturer | 1 | December 10, 2015 | 0 | 0 | 0 | api.fda.gov |
| Armorlink SH Corp | ShangHai, China | Contract manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Amphenol Medical Technologies (Dongguan) Co., Ltd. | Dongguan Guangdong, China | Contract manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Tontec Precision Plastics Technology (shenzhen) Co. Ltd. | Shenzhen Guangdong, China | Contract manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Tianjin Choice Medical Device Co., Ltd. | Tianjin, China | Contract manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| VTech Communications Ltd | DONGGUAN Guangdong, China | Contract manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Wuhan Strong Electronics | Wuhan Hubei, 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.