Taiwan FDA registration d7a10ac5adb8c60f4c88a26de427a078
Eveline Ovulation Test System (Non-Sterile)
TW: 伊必測 排卵檢測系統 (未滅菌)
Taiwan·Risk Class 1·MD·Inner Lake Plant of AXA Shengke Co., Ltd·Registered Jun 28, 2017 – Jun 28, 2027ActiveRegistration details
- Analysis ID
- d7a10ac5adb8c60f4c88a26de427a078
- License Form
- Ministry of Health Medical Device Manufacturing No. 006812
Company information
- Manufacturer
- Inner Lake Plant of AXA Shengke Co., Ltd
- Manufacturer Country
- Taiwan, Province of China
- Authorized Representative
- IXENSOR 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)
- A1485 Progesterone Test System
- Import Information
- Produced in Taiwan, China
Dates and status
- Registration Date
- Jun 28, 2017
- Expiry Date
- Jun 28, 2027
About this record
Access comprehensive regulatory information for Eveline Ovulation Test System (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 d7a10ac5adb8c60f4c88a26de427a078 and manufactured by Inner Lake Plant of AXA Shengke Co., Ltd. The authorized representative in Taiwan is IXENSOR 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.
Free DatabasePowered by Pure Global AI89,000+ Devices