Taiwan FDA registration 923254d847376d7bf301121047c68b12
"ARTRON" FSH TEST (Non-Sterile)
TW: "雅昌"卵泡刺激激素檢測試劑 (未滅菌)
Taiwan·Risk Class 1·MD·ARTRON LABORATORIES INC.·Registered Mar 01, 2016 – Mar 01, 2026ExpiredRegistration details
- Analysis ID
- 923254d847376d7bf301121047c68b12
- License Form
- Ministry of Health Medical Device Import No. 016209
- Customs Code
- DHA09401620909
Company information
- Manufacturer
- ARTRON LABORATORIES INC.
- Manufacturer Country
- Canada
- Authorized Representative
- GORED ENTERPRISE CO., LTD.
Product details
- Intended Use
- Limited to the first level recognition range of the follicle-stimulating hormone test system (A.1300) of the management method of medical equipment.
- Product Type (Level 1)
- A Clinical chemistry and clinical toxicology
- Product Type (Level 2)
- A1300 Follicle-stimulating hormone testing system
- Import Information
- Imported from abroad
Dates and status
- Registration Date
- Mar 01, 2016
- Expiry Date
- Mar 01, 2026
About this record
Access comprehensive regulatory information for "ARTRON" FSH 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 923254d847376d7bf301121047c68b12 and manufactured by ARTRON LABORATORIES INC.. The authorized representative in Taiwan is GORED ENTERPRISE CO., LTD..
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