Taiwan FDA registration 3723508e7eb91a341dbaf2baa3247d6a
"Edward" Ovulation Rapid Test Reagent (Unsterilized)
TW: "艾德" 排卵快速檢測試劑 (未滅菌)
Taiwan·Risk Class 1·AIDE DIAGNOSTIC CO., LTD.·Registered Sep 05, 2016 – Sep 05, 2021CancelledRegistration details
- Analysis ID
- 3723508e7eb91a341dbaf2baa3247d6a
- Customs Code
- DHA09600284705
Company information
- Manufacturer
- AIDE DIAGNOSTIC CO., LTD.
- Manufacturer Country
- China
- Authorized Representative
- WinBaby Co.
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
- Input;; Chinese goods
Dates and status
- Registration Date
- Sep 05, 2016
- Expiry Date
- Sep 05, 2021
- Cancellation Date
- Sep 19, 2023
Cancellation information
- Status
- Logged out
- Reason
- 自行鍵入
About this record
Access comprehensive regulatory information for "Edward" Ovulation Rapid Test Reagent (Unsterilized) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number 3723508e7eb91a341dbaf2baa3247d6a and manufactured by AIDE DIAGNOSTIC CO., LTD.. The authorized representative in Taiwan is WinBaby Co..
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