Taiwan FDA registration bbccdc85d01eab44876b8067c75c4c85
“FIBERPURE” Hollow Fiber Dialyzer
TW: “禾研”中空纖維透析器
Taiwan·Risk Class 2·MD·Heyan Technology Co., Ltd·Registered Nov 03, 2016 – Nov 03, 2021CancelledRegistration details
- Analysis ID
- bbccdc85d01eab44876b8067c75c4c85
- License Form
- Ministry of Health Medical Device Manufacturing No. 005464
Company information
- Manufacturer
- Heyan Technology Co., Ltd
- Manufacturer Country
- Taiwan, Province of China
- Authorized Representative
- Heyan Technology Co., Ltd
Product details
- Product Type (Level 1)
- H Gastroenterology-urology devices
- Product Type (Level 2)
- H5860 Highly permeable hemodialysis system
- Import Information
- Produced in Taiwan, China
Dates and status
- Registration Date
- Nov 03, 2016
- Expiry Date
- Nov 03, 2021
- Cancellation Date
- Aug 04, 2023
Cancellation information
- Status
- Logged out
- Reason
- 許可證已逾有效期
About this record
Access comprehensive regulatory information for “FIBERPURE” Hollow Fiber Dialyzer in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number bbccdc85d01eab44876b8067c75c4c85 and manufactured by Heyan Technology Co., Ltd. The authorized representative in Taiwan is Heyan Technology Co., Ltd.
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