Taiwan FDA registration 805554963fa2ac36e622eb8cb187593f
"WEIYOU" Ovulation Test (Non-Sterile)
TW: "微友" 排卵測試筆 (未滅菌)
Taiwan·Risk Class 1·MD·SPD SWISS PRECISION DIAGNOSTICS GMBH·Registered Feb 25, 2021 – Feb 25, 2026ExpiredRegistration details
- Analysis ID
- 805554963fa2ac36e622eb8cb187593f
- License Form
- Ministry of Health Medical Device Import No. 022337
- Customs Code
- DHA09402233704
Company information
- Manufacturer
- SPD SWISS PRECISION DIAGNOSTICS GMBH
- Manufacturer Country
- Switzerland
- Authorized Representative
- WEIYOU TECH INC.
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
- Feb 25, 2021
- Expiry Date
- Feb 25, 2026
About this record
Access comprehensive regulatory information for "WEIYOU" 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 805554963fa2ac36e622eb8cb187593f and manufactured by SPD SWISS PRECISION DIAGNOSTICS GMBH. The authorized representative in Taiwan is WEIYOU TECH INC..
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