Taiwan FDA registration fe1a5f191688ad88f5992e96b6f27749
Yilitest LOHAS blood ketone test strip (unsterilized)
TW: 易立測 樂活 血酮試紙 (未滅菌)
Taiwan·Risk Class 1·BIOPTIK TECHNOLOGY, INC.·Registered Jan 08, 2020 – Jan 08, 2030ActiveRegistration details
- Analysis ID
- fe1a5f191688ad88f5992e96b6f27749
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
- Jan 08, 2020
- Expiry Date
- Jan 08, 2030
About this record
Access comprehensive regulatory information for Yilitest LOHAS blood ketone test strip (unsterilized) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number fe1a5f191688ad88f5992e96b6f27749 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