Taiwan FDA registration 7966b6091b580e8a02d16d0f9318b142
FlexTest LOHAS Blood Ketone Monitoring System (Unsterilized)
TW: 易立測 樂活 血酮 監測系統 (未滅菌)
Taiwan·Risk Class 1·BIOPTIK TECHNOLOGY, INC.·Registered Dec 08, 2021 – Dec 08, 2026ActiveRegistration details
- Analysis ID
- 7966b6091b580e8a02d16d0f9318b142
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 "Ketone (non-quantitative) test system (A.1435)" first level identification range.
- Product Type (Level 1)
- A Clinical chemistry and clinical toxicology
- Product Type (Level 2)
- A.1435 Ketone (non-quantitative) testing system
- Import Information
- 國產;; QMS/QSD
Dates and status
- Registration Date
- Dec 08, 2021
- Expiry Date
- Dec 08, 2026
About this record
Access comprehensive regulatory information for FlexTest LOHAS Blood Ketone 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 7966b6091b580e8a02d16d0f9318b142 and manufactured by BIOPTIK TECHNOLOGY, INC.. The authorized representative in Taiwan is BIOPTIK TECHNOLOGY, INC..
This page provides complete technical specifications, regulatory compliance details. Pure Global AI offers free access to 89,000+ Taiwan medical device registrations, helping global MedTech companies navigate Taiwan FDA regulations, identify competitors, and discover partnership opportunities efficiently.
Free DatabasePowered by Pure Global AI89,000+ Devices