Taiwan FDA registration 44da0e4c5589fcf83a4aad37fc695544
Lighter Ovulation Test (Unsterilized)
TW: 萊特兒排卵檢測片(未滅菌)
Registration details
- Analysis ID
- 44da0e4c5589fcf83a4aad37fc695544
- Customs Code
- DHA09600337406
Company information
- Manufacturer
- Nantong Egens Biotechnology Co.,LTD
- Manufacturer Country
- China
- Authorized Representative
- BONRAYBIO CO., LTD.
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)
- A.1485 Progesterone testing system
- Import Information
- Chinese goods;; input
Dates and status
- Registration Date
- Mar 12, 2018
- Expiry Date
- Mar 12, 2023
About this record
Access comprehensive regulatory information for Lighter Ovulation Test (Unsterilized) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number 44da0e4c5589fcf83a4aad37fc695544 and manufactured by Nantong Egens Biotechnology Co.,LTD. The authorized representative in Taiwan is BONRAYBIO CO., LTD..
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.
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