Taiwan FDA registration 6c853efde8564b9740beb50071e3d1f2
Bajie Heme Tube Solution (Unsterilized)
TW: 百捷 血紅素品管液 (未滅菌)
Taiwan·Risk Class 1·Qinli Biotechnology Co., Ltd. new tree factory·Registered Dec 24, 2015 – Dec 24, 2025ExpiredRegistration details
- Analysis ID
- 6c853efde8564b9740beb50071e3d1f2
Company information
- Manufacturer
- Qinli Biotechnology Co., Ltd. new tree factory
- Manufacturer Country
- Taiwan, Province of China
- Authorized Representative
- GENERAL LIFE BIOTECHNOLOGY CO., LTD.
Product details
- Intended Use
- Limited to the classification and grading management of medical equipment, quality control materials (analytical and non-analytical) (A.1660) the first level identification range.
- 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
- Domestic
Dates and status
- Registration Date
- Dec 24, 2015
- Expiry Date
- Dec 24, 2025
About this record
Access comprehensive regulatory information for Bajie Heme Tube 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 6c853efde8564b9740beb50071e3d1f2 and manufactured by Qinli Biotechnology Co., Ltd. new tree factory. The authorized representative in Taiwan is GENERAL LIFE BIOTECHNOLOGY CO., LTD..
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