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Data / Medical devices / Enteral Administration Kit (Adult & Pediatric) / China

FDA-registered makers of Enteral Administration Kit (Adult & Pediatric) in China: 6 establishments

6 establishments in China are registered with the FDA to make Enteral Administration Kit (Adult & Pediatric) (product code PRM). 0 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
Enteral Administration Kit (Adult & Pediatric)
Product code
PRM
Country
China

Makers of Enteral Administration Kit (Adult & Pediatric) in China

MakerLocationRole510(k) clearancesLatest clearancePMA approvalsRecall eventsClass ISource
Amsino Medical (kunshan) Co., Ltd.KUNSHAN CITY Jiangsu, ChinaContract manufacturer, Manufacturer0000api.fda.gov
Boen Healthcare Co., Ltd.Suzhou Jiangsu, ChinaExporter to the US, Specification developer0000api.fda.gov
Evereast Medical Products Group Co., LtdChangyuan City Henan, ChinaContract manufacturer, Exporter to the US, Manufacturer0000api.fda.gov
Ningbo Hanyue Medical Technology Co.,ltdCIXI CITY Zhejiang, ChinaContract manufacturer, Exporter to the US, Manufacturer0000api.fda.gov
Ningbo Luke Medical Devices Co., Ltd.Yuyao Zhejiang, ChinaContract manufacturer, Exporter to the US, Manufacturer0000api.fda.gov
Shandong Zhushi Pharmaceutical Group Co., LtdHeze 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.