Taiwan FDA registration 3bf5644fc86039d4ef90cf0aabc40e5d
Yilitest II Glucose Tube Solution (Unsterilized)
TW: 易立測II 葡萄糖品管液 (未滅菌)
Taiwan·Risk Class 1·BIOPTIK TECHNOLOGY, INC.·Registered Nov 17, 2011 – Nov 17, 2026ActiveRegistration details
- Analysis ID
- 3bf5644fc86039d4ef90cf0aabc40e5d
Company information
- Manufacturer
- BIOPTIK TECHNOLOGY, INC.
- Manufacturer Country
- Taiwan, Province of China
- Authorized Representative
- BIOPTIK TECHNOLOGY, INC.
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
- QMS/QSD;; 國產
Dates and status
- Registration Date
- Nov 17, 2011
- Expiry Date
- Nov 17, 2026
About this record
Access comprehensive regulatory information for Yilitest II Glucose 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 3bf5644fc86039d4ef90cf0aabc40e5d and manufactured by BIOPTIK TECHNOLOGY, INC.. The authorized representative in Taiwan is BIOPTIK TECHNOLOGY, INC..
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