Taiwan FDA registration fe6bc671e51be603f60b20d0a39f95de
"Artron" Ovulation Test Reagent (Unsterilized)
TW: "雅創" 排卵檢測試劑 (未滅菌)
Taiwan·Risk Class 1·HANGZHOU ALLTEST BIOTECH CO., LTD.·Registered Oct 02, 2023 – Oct 02, 2028ActiveRegistration details
- Analysis ID
- fe6bc671e51be603f60b20d0a39f95de
- Customs Code
- DHA09600483100
Company information
- Manufacturer
- HANGZHOU ALLTEST BIOTECH CO., LTD.
- Manufacturer Country
- China
- Authorized Representative
- GORED ENTERPRISE CO., LTD.
Product details
- Intended Use
- Limited to the classification and grading management measures of medical equipment "Luteinizing hormone test system (A.1485)" first level identification range.
- Product Type (Level 1)
- A Clinical chemistry and clinical toxicology
- Product Type (Level 2)
- A.1485 Progesterone testing system
- Import Information
- Chinese goods;; Input;; QMS/QSD
Dates and status
- Registration Date
- Oct 02, 2023
- Expiry Date
- Oct 02, 2028
About this record
Access comprehensive regulatory information for "Artron" Ovulation Test Reagent (Unsterilized) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number fe6bc671e51be603f60b20d0a39f95de and manufactured by HANGZHOU ALLTEST BIOTECH CO., LTD.. The authorized representative in Taiwan is GORED ENTERPRISE CO., LTD..
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