Taiwan FDA registration ece102f3a8538357db4393224d5ce55c
"Dibao" glucose quality control solution (unsterilized)
TW: 〝帝寶〞葡萄糖品管液 (未滅菌)
Taiwan·Risk Class 1·Heshi Biomedical Technology Co., Ltd. Zhonghe No. 2 Factory·Registered Jan 29, 2013 – Jan 29, 2023CancelledRegistration details
- Analysis ID
- ece102f3a8538357db4393224d5ce55c
Company information
- Manufacturer Country
- Taiwan, Province of China
- Authorized Representative
- HEALTH & LIFE CO., LTD.
Product details
- Intended Use
- Limited to the first level identification range of quality control materials (analytical and non-analytical) (A.1660) of the Measures for the Administration of Medical Devices.
- Product Type (Level 1)
- A Clinical chemistry and clinical toxicology
- Product Type (Level 2)
- A.1660 Quality control materials (analytical and non-analytical)
- Import Information
- 國產;; QMS/QSD
Dates and status
- Registration Date
- Jan 29, 2013
- Expiry Date
- Jan 29, 2023
- Cancellation Date
- Apr 15, 2019
Cancellation information
- Status
- Logged out
- Reason
- 公司歇業
About this record
Access comprehensive regulatory information for "Dibao" glucose quality control solution (unsterilized) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number ece102f3a8538357db4393224d5ce55c and manufactured by Heshi Biomedical Technology Co., Ltd. Zhonghe No. 2 Factory. The authorized representative in Taiwan is HEALTH & LIFE CO., LTD..
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