Taiwan FDA registration e3a7adb4b96dfbfcd92387f52289f965
"Guowei" human serum dry powder (unsterilized)
TW: “國維”人體血清乾粉 (未滅菌)
Taiwan·Risk Class 1·Guowei United Technology Co., Ltd·Registered Mar 04, 2013 – Mar 04, 2018CancelledRegistration details
- Analysis ID
- e3a7adb4b96dfbfcd92387f52289f965
Company information
- Manufacturer
- Guowei United Technology Co., Ltd
- Manufacturer Country
- Taiwan, Province of China
- Authorized Representative
- Guowei United Technology Co., Ltd
Product details
- Intended Use
- It is limited to the first level of identification scope of animal and human serum (B.2800) of the Administrative Measures for Medical Devices.
- Product Type (Level 1)
- B Hematology, pathology, and genetics
- Product Type (Level 2)
- B.2800 Animal and human serum
- Import Information
- Domestic
Dates and status
- Registration Date
- Mar 04, 2013
- Expiry Date
- Mar 04, 2018
- Cancellation Date
- Nov 04, 2019
Cancellation information
- Status
- Logged out
- Reason
- 許可證已逾有效期
About this record
Access comprehensive regulatory information for "Guowei" human serum dry powder (unsterilized) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number e3a7adb4b96dfbfcd92387f52289f965 and manufactured by Guowei United Technology Co., Ltd. The authorized representative in Taiwan is Guowei United Technology Co., Ltd.
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.
Free DatabasePowered by Pure Global AI89,000+ Devices