Taiwan FDA registration 485f5e239fc3ea0f5f6351c4480e996a
FlexTest Eulive Triglyceride Monitoring System (Unsterilized)
TW: 易立測 優活 三酸甘油酯 監測系統 (未滅菌)
Registration details
- Analysis ID
- 485f5e239fc3ea0f5f6351c4480e996a
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, triglycerides test system (A.1705) first grade identification range.
- Product Type (Level 1)
- A Clinical chemistry and clinical toxicology
- Product Type (Level 2)
- A.1705 Triglyceride Test System
- Import Information
- QMS/QSD;; 國產
Dates and status
- Registration Date
- Sep 16, 2019
- Expiry Date
- Sep 16, 2029
About this record
Access comprehensive regulatory information for FlexTest Eulive Triglyceride Monitoring System (Unsterilized) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number 485f5e239fc3ea0f5f6351c4480e996a and manufactured by BIOPTIK TECHNOLOGY, INC.. The authorized representative in Taiwan is BIOPTIK TECHNOLOGY, INC..
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