Taiwan FDA registration cb63bd6156ec172b195e511c4d7d788f
"SPD" 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 01, 2016 – Feb 01, 2021ExpiredRegistration details
- Analysis ID
- cb63bd6156ec172b195e511c4d7d788f
- License Form
- Ministry of Health Medical Device Import No. 016135
- Customs Code
- DHA09401613506
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 01, 2016
- Expiry Date
- Feb 01, 2021
About this record
Access comprehensive regulatory information for "SPD" 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 cb63bd6156ec172b195e511c4d7d788f and manufactured by SPD SWISS PRECISION DIAGNOSTICS GMBH. The authorized representative in Taiwan is WEIYOU TECH INC..
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