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Data / Medical devices / Saline, Vascular Access Flush / China

FDA-registered makers of Saline, Vascular Access Flush in China: 7 establishments

7 establishments in China are registered with the FDA to make Saline, Vascular Access Flush (product code NGT). 4 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
Saline, Vascular Access Flush
Product code
NGT
Country
China

Makers of Saline, Vascular Access Flush in China

MakerLocationRole510(k) clearancesLatest clearancePMA approvalsRecall eventsClass ISource
Amsino Medical (kunshan) Co., Ltd.KUNSHAN CITY Jiangsu, ChinaManufacturer, Specification developer2March 22, 2022000api.fda.gov
Anhui Tiankang Medical Technology Co., Ltd.Tianchang Anhui, ChinaManufacturer1August 12, 2023000api.fda.gov
Anhui Tianyang Pharmaceutical Co., LtdTianchang Anhui, ChinaManufacturer1August 12, 2023000api.fda.gov
Hantech Medical Device Co., Ltd.Cixi Zhejiang, ChinaManufacturer1September 27, 2023000api.fda.gov
Hantech (ningbo) Medical Technology Co., Ltd.Ningbo Zhejiang, ChinaContract manufacturer0000api.fda.gov
Jiaxing Tianhe Pharmaceutical Co., Ltd.Jiaxing Zhejiang, ChinaContract manufacturer0000api.fda.gov
Jinan Babio Biotechnology Co.,ltd.Jinan City Shandong, ChinaExporter to the US, 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.