Taiwan FDA registration f002cf0739ec0c5ab00215bd0cc4f355
IF Ovulation(LH) Rapid Test (Non-sterile)
TW: 依芙 排卵檢測試劑 (未滅菌)
Taiwan·Risk Class 1·MD·FIRSTEP BIORESEARCH INC.·Registered Feb 23, 2017 – Feb 23, 2027ActiveRegistration details
- Analysis ID
- f002cf0739ec0c5ab00215bd0cc4f355
- License Form
- Ministry of Health Medical Device Manufacturing No. 006605
Company information
- Manufacturer
- FIRSTEP BIORESEARCH INC.
- Manufacturer Country
- Taiwan, Province of China
- Authorized Representative
- FIRSTEP BIORESEARCH INC.
Product details
- Intended Use
- Limited to the first level recognition range of the "Luteinizing hormone test system (A.1485)" of the Measures for the Administration of Medical Devices.
- Product Type (Level 1)
- A Clinical chemistry and clinical toxicology
- Product Type (Level 2)
- A1485 Progesterone Test System
- Import Information
- Produced in Taiwan, China
Dates and status
- Registration Date
- Feb 23, 2017
- Expiry Date
- Feb 23, 2027
About this record
Access comprehensive regulatory information for IF Ovulation(LH) Rapid Test (Non-sterile) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number f002cf0739ec0c5ab00215bd0cc4f355 and manufactured by FIRSTEP BIORESEARCH INC.. The authorized representative in Taiwan is FIRSTEP BIORESEARCH 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