Taiwan FDA registration 4cf0f31a903c63363630ae506dc76472
"SPD" Clearblue Ovulation Test (Non-Sterile)
TW: "速必得"排卵測試筆(未滅菌)
Taiwan·Risk Class 1·MD·SPD Swiss Precision Diagnostics GmbH·Registered Jul 03, 2018 – Jul 03, 2023ExpiredRegistration details
- Analysis ID
- 4cf0f31a903c63363630ae506dc76472
- License Form
- Ministry of Health Medical Device Import No. 019258
- Customs Code
- DHA09401925801
Company information
- Manufacturer
- SPD Swiss Precision Diagnostics GmbH
- Manufacturer Country
- Switzerland
- 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)
- A1485 Progesterone Test System
- Import Information
- Imported from abroad
Dates and status
- Registration Date
- Jul 03, 2018
- Expiry Date
- Jul 03, 2023
About this record
Access comprehensive regulatory information for "SPD" Clearblue Ovulation Test (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 4cf0f31a903c63363630ae506dc76472 and manufactured by SPD Swiss Precision Diagnostics GmbH. The authorized representative in Taiwan is SUNGYIN BIO INTERNATIONAL CO., LTD..
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