Taiwan FDA registration 635c5541fb94f5104aeae044048cf66a
"JIREH" Clearblue Ovulation Test (Non-Sterile)
TW: "以樂" 排卵測試筆 (未滅菌)
Taiwan·Risk Class 1·MD·SPD Swiss Precision Diagnostics GmbH·Registered Jul 04, 2019 – Jul 04, 2024ExpiredRegistration details
- Analysis ID
- 635c5541fb94f5104aeae044048cf66a
- License Form
- Ministry of Health Medical Device Import No. 020621
- Customs Code
- DHA09402062104
Company information
- Manufacturer
- SPD Swiss Precision Diagnostics GmbH
- Manufacturer Country
- Switzerland
- Authorized Representative
- JEHOVAH-JIREH ENTERPRISE 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 04, 2019
- Expiry Date
- Jul 04, 2024
About this record
Access comprehensive regulatory information for "JIREH" 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 635c5541fb94f5104aeae044048cf66a and manufactured by SPD Swiss Precision Diagnostics GmbH. The authorized representative in Taiwan is JEHOVAH-JIREH ENTERPRISE CO., LTD..
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