Taiwan FDA registration 6c14ef4e13942212a36032877147bbcd
"AXA" progesterone ovulation test kit (unsterilized)
TW: "安盛" 黃體素檢測排卵試劑盒(未滅菌)
Taiwan·Risk Class 1·IXENSOR CO., LTD.·Registered Jun 17, 2016 – Jun 17, 2021CancelledRegistration details
- Analysis ID
- 6c14ef4e13942212a36032877147bbcd
Company information
- Manufacturer
- IXENSOR 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)
- A.1485 Progesterone testing system
- Import Information
- Domestic
Dates and status
- Registration Date
- Jun 17, 2016
- Expiry Date
- Jun 17, 2021
- Cancellation Date
- Dec 06, 2017
Cancellation information
- Status
- Logged out
- Reason
- 自行鍵入
About this record
Access comprehensive regulatory information for "AXA" progesterone ovulation test kit (unsterilized) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number 6c14ef4e13942212a36032877147bbcd and manufactured by IXENSOR CO., LTD.. The authorized representative in Taiwan is IXENSOR CO., LTD..
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