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Data / Medical devices / Filter, Bacterial, Breathing-Circuit / China

FDA-registered makers of Filter, Bacterial, Breathing-Circuit in China: 12 establishments

12 establishments in China are registered with the FDA to make Filter, Bacterial, Breathing-Circuit (product code CAH). 6 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
Filter, Bacterial, Breathing-Circuit
Product code
CAH
Country
China

Makers of Filter, Bacterial, Breathing-Circuit in China

MakerLocationRole510(k) clearancesLatest clearancePMA approvalsRecall eventsClass ISource
Zhejiang Haisheng Medical Device Co., Ltd.Shaoxing Zhejiang, ChinaContract manufacturer, Manufacturer2December 18, 2015000api.fda.gov
GVS Technology (Suzhou) Co., LtdSuzhou Jiangsu, ChinaContract manufacturer, Manufacturer1May 13, 2004000api.fda.gov
Ningbo Huakun Medical Equipment Co.,ltdCixi Zhejiang, ChinaManufacturer1February 8, 2023000api.fda.gov
Shaoxing Haitech Medical Products Co., LtdSHAOXING Zhejiang, ChinaManufacturer1February 15, 2024000api.fda.gov
Vincent Medical (dong Guan) Manufacturing Co., Ltd.Dong Guan City Guangdong, ChinaContract manufacturer, Manufacturer1June 24, 1997000api.fda.gov
VR Medical Technology Co., Ltd.KUNSHAN Jiangsu, ChinaManufacturer1July 30, 2014000api.fda.gov
Amsino Medical (shanghai) Co., Ltd.Shanghai, ChinaContract manufacturer0000api.fda.gov
Conod Medical Co.,LimitedChangshu Jiangsu, ChinaContract manufacturer0000api.fda.gov
Flexicare Medical (dongguan) Ltd.DONGGUAN CITY Guangdong, ChinaContract manufacturer0000api.fda.gov
GaleMed (Xiamen) Co., Ltd.XIAMEN Fujian, ChinaContract manufacturer0000api.fda.gov
Intersurgical Medical Apparatus (changzhou) Co., Ltd.Changzhou City Jiangsu, ChinaContract manufacturer0000api.fda.gov
Sunmed Ap, Ltd.ZHUHAI Guangdong, ChinaContract manufacturer0000api.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.