Taiwan FDA registration 1fdb0dd4d916a3a5f1b56df22679771c
"Yinghemei" blood purification kit
TW: “英禾美”血液淨化套組
Taiwan·Risk Class 2·Yinghe Mei Biomedical Co., Ltd.;; Shengte Technology Co., Ltd. Yike Factory·Registered Nov 12, 2019 – Nov 12, 2029ActiveRegistration details
- Analysis ID
- 1fdb0dd4d916a3a5f1b56df22679771c
Company information
- Manufacturer Country
- Taiwan, Province of China
- Authorized Representative
- HEMOSCIEN CORPORATION
Product details
- Intended Use
- For details, it is Chinese approved copy of the imitation order
- Product Type (Level 1)
- H Gastroenterology and urology
- Product Type (Level 2)
- H.5540 Blood Access Devices and Accessories
- Import Information
- Domestic;; Contract manufacturing
Dates and status
- Registration Date
- Nov 12, 2019
- Expiry Date
- Nov 12, 2029
About this record
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.
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