Taiwan FDA registration e403fba15f5624c62ddad7fd48f2135d
Inhome adsorber
TW: 英禾美吸附器
Taiwan·Risk Class 3·Shengte Technology Co., Ltd.;; Yinghe Mei Biomedical Co., Ltd·Registered Jan 13, 2012 – Jan 13, 2027ActiveRegistration details
- Analysis ID
- e403fba15f5624c62ddad7fd48f2135d
- Customs Code
- DHY00500356901
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.5870 吸附式血液灌注系統
- Import Information
- Domestic;; Contract manufacturing
Dates and status
- Registration Date
- Jan 13, 2012
- Expiry Date
- Jan 13, 2027
About this record
Access comprehensive regulatory information for Inhome adsorber in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 3 medical device is registered under number e403fba15f5624c62ddad7fd48f2135d and manufactured by Shengte Technology Co., Ltd.;; Yinghe Mei Biomedical Co., Ltd. The authorized representative in Taiwan is HEMOSCIEN CORPORATION.
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