Data / Medical devices / Electrode, Electrocardiograph / China

FDA-registered makers of Electrode, Electrocardiograph in China: 29 establishments

Name: FDA-registered makers of Electrode, Electrocardiograph in China
Creator: SpecStream
License: https://creativecommons.org/licenses/by/4.0/

29 establishments in China are registered with the FDA to make Electrode, Electrocardiograph (product code DRX). 3 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: Electrode, Electrocardiograph
Product code: DRX
Country: China

Makers of Electrode, Electrocardiograph in China

Maker	Location	Role	510(k) clearances	Latest clearance	Source
Bio Protech Yantai Inc	Yantai Shandong, China	Manufacturer	4	November 7, 2008	api.fda.gov
Shanghai Intco Electrode Manufacturing Co Ltd	Shanghai, China	Exporter to the US, Manufacturer	2	May 10, 2010	api.fda.gov
Unimed Medical Supplies Inc	Shenzhen Guangdong, China	Exporter to the US, Manufacturer	1	September 15, 2004	api.fda.gov
Apk Technology Co., Ltd	Shenzhen Guangdong, China	Exporter to the US, Manufacturer	0		api.fda.gov
Baisheng Medical Co.,ltd.	JIANGMEN Guangdong, China	Manufacturer	0		api.fda.gov
Boen Healthcare Co., Ltd.	Suzhou Jiangsu, China	Exporter to the US, Specification developer	0		api.fda.gov
China Qingdao Bright Medical Manufacturing Co.,ltd.	Qingdao Shandong, China	Contract manufacturer, Manufacturer	0		api.fda.gov
Cathay Manufacturing Corp.	Shanghai, China	Contract manufacturer, Exporter to the US, Manufacturer	0		api.fda.gov
Dongguan Quanding Medical Supplies Co., Ltd	Dongguan Guangdong, China	Manufacturer	0		api.fda.gov
Dongguan Ruibaolian Medical Science & Technology Co., Ltd	Dongguan Guangdong, China	Contract manufacturer, Specification developer	0		api.fda.gov
Huzhou Junda Industry Co., Ltd.	Anji Zhejiang, China	Contract manufacturer, Exporter to the US, Manufacturer	0		api.fda.gov
Jiangsu Andycare Medical Products Co.,ltd.	Zhenjiang Jiangsu, China	Contract manufacturer, Exporter to the US, Manufacturer	0		api.fda.gov
Linxens Healthcare (Tianjin) Co., Ltd	JinNan District Tianjin, China	Contract manufacturer	0		api.fda.gov
Meetu Technology (shenzhen) Co., Ltd	Shenzhen Guangdong, China	Contract manufacturer, Repackager or relabeler	0		api.fda.gov
Ningbo Chibanda Imp &exp Co, Ltd	Ningbo Zhejiang, China	Manufacturer	0		api.fda.gov
Ningbo Greetmed Medical Instruments Co., Ltd.	Ningbo Zhejiang, China	Exporter to the US, Specification developer	0		api.fda.gov
Ningbo Hanyue Medical Technology Co.,ltd	CIXI CITY Zhejiang, China	Contract manufacturer, Exporter to the US, Manufacturer	0		api.fda.gov
Orantech Inc.	Shenzhen Guangdong, China	Exporter to the US, Manufacturer	0		api.fda.gov
Philips (China) Investment Co., Ltd. Philips Healthcare - Shanghai CDC	Shanghai, China	Specification developer	0		api.fda.gov
Shandong Intco Medical Products Co Ltd	Qingzhou Shandong, China	Manufacturer	0		api.fda.gov
Shanghai Yuechen Medical Supply Co..ltd.	Shanghai, China	Contract manufacturer, Exporter to the US, Manufacturer	0		api.fda.gov
Shenzhen Coreray Technology Co., Ltd.	Shenzhen Guangdong, China	Manufacturer	0		api.fda.gov
Shenzhen Launch Electrical Co., Ltd	Shenzhen Guangdong, China	Manufacturer	0		api.fda.gov
Shenzhen Med-Link Electronics Tech Co.,ltd	Shenzhen Guangdong, China	Manufacturer	0		api.fda.gov
Suzhou Ennova Electronic Technology Co Ltd	Suzhou Jiangsu, China	Exporter to the US, Manufacturer	0		api.fda.gov
Suzhou Letai Medical Technology Co.,ltd.	Suzhou Jiangsu, China	Manufacturer	0		api.fda.gov
Top-rank Health Care Co.,Ltd.	Shaoxing Zhejiang, China	Manufacturer	0		api.fda.gov
Voncare Medical Device Co Ltd	Huizhou Guangdong, China	Manufacturer	0		api.fda.gov
Zhejiang Mediunion Healthcare Group Co.,ltd	Ningbo Zhejiang, China	Manufacturer	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.