Taiwan FDA registration 0d131d7337311eb28ced1dd7e3d90547
"Naidan" Ovulation Rapid Test Reagent (Unsterilized)
TW: "奈當" 排卵快速檢測試劑 (未滅菌)
Taiwan·Risk Class 1·NANTONG DIAGNOS BIOTECHNOLOGY CO., LTD.·Registered Mar 14, 2017 – Mar 14, 2022CancelledRegistration details
- Analysis ID
- 0d131d7337311eb28ced1dd7e3d90547
- Customs Code
- DHA09600302102
Company information
- Manufacturer
- NANTONG DIAGNOS BIOTECHNOLOGY CO., LTD.
- Manufacturer Country
- China
- Authorized Representative
- SUNGYIN BIO INTERNATIONAL 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
- Input;; Chinese goods
Dates and status
- Registration Date
- Mar 14, 2017
- Expiry Date
- Mar 14, 2022
- Cancellation Date
- Apr 12, 2024
Cancellation information
- Status
- Logged out
- Reason
- 許可證已逾有效期
About this record
Access comprehensive regulatory information for "Naidan" 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 0d131d7337311eb28ced1dd7e3d90547 and manufactured by NANTONG DIAGNOS BIOTECHNOLOGY CO., LTD.. The authorized representative in Taiwan is SUNGYIN BIO INTERNATIONAL CO., LTD..
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