Taiwan FDA registration 8b1e341a0474ed691e25806ff87377dc
Ekang Ketone Liquid (Unsterilized)
TW: 易康 酮體品管液 (未滅菌)
Taiwan·Risk Class 1·BIOPTIK TECHNOLOGY, INC.·Registered Aug 21, 2019 – Aug 21, 2029ActiveRegistration details
- Analysis ID
- 8b1e341a0474ed691e25806ff87377dc
Company information
- Manufacturer
- BIOPTIK TECHNOLOGY, INC.
- Manufacturer Country
- Taiwan, Province of China
- Authorized Representative
- EASY LIFE GREEN TECHNOLOGY CORPORATION
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
- 國產;; 委託製造;; QMS/QSD
Dates and status
- Registration Date
- Aug 21, 2019
- Expiry Date
- Aug 21, 2029
About this record
Access comprehensive regulatory information for Ekang Ketone Liquid (Unsterilized) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number 8b1e341a0474ed691e25806ff87377dc and manufactured by BIOPTIK TECHNOLOGY, INC.. The authorized representative in Taiwan is EASY LIFE GREEN TECHNOLOGY CORPORATION.
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