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"Yinghemei" blood purification kit - Taiwan Registration 1fdb0dd4d916a3a5f1b56df22679771c

Access comprehensive regulatory information for "Yinghemei" blood purification kit in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 1fdb0dd4d916a3a5f1b56df22679771c and manufactured by Yinghe Mei Biomedical Co., Ltd.;; Shengte Technology Co., Ltd. Yike Factory. The authorized representative in Taiwan is HEMOSCIEN CORPORATION.

This page provides complete technical specifications, regulatory compliance details. Pure Global AI offers free access to 89,000+ Taiwan medical device registrations, helping global MedTech companies navigate Taiwan FDA regulations, identify competitors, and discover partnership opportunities efficiently.

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1fdb0dd4d916a3a5f1b56df22679771c
Registration Details
Taiwan FDA Registration: 1fdb0dd4d916a3a5f1b56df22679771c
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Device Details

"Yinghemei" blood purification kit
TW: โ€œ่‹ฑ็ฆพ็พŽโ€่ก€ๆถฒๆทจๅŒ–ๅฅ—็ต„
Risk Class 2

Registration Details

1fdb0dd4d916a3a5f1b56df22679771c

Company Information

Product Details

For details, it is Chinese approved copy of the imitation order

H Gastroenterology and urology

H.5540 Blood Access Devices and Accessories

Domestic;; Contract manufacturing

Dates and Status

Nov 12, 2019

Nov 12, 2029