Taiwan FDA registration f4fa9eb85b278a38d63a67a469ead0aa
"PIIP" ovulation detection reagent (unsterilized)
TW: "博拓" 排卵檢測試劑 (未滅菌)
Taiwan·Risk Class 1·HANGZHOU BIOTEST BIOTECH CO., LTD.·Registered Jul 26, 2017 – Jul 26, 2027ActiveRegistration details
- Analysis ID
- f4fa9eb85b278a38d63a67a469ead0aa
- Customs Code
- DHA09600315902
Company information
- Manufacturer
- HANGZHOU BIOTEST BIOTECH CO., LTD.
- Manufacturer Country
- China
- Authorized Representative
- GENERAL BIOLOGICALS CORP.
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
- Input;; Chinese goods
Dates and status
- Registration Date
- Jul 26, 2017
- Expiry Date
- Jul 26, 2027
About this record
Access comprehensive regulatory information for "PIIP" ovulation detection 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 f4fa9eb85b278a38d63a67a469ead0aa and manufactured by HANGZHOU BIOTEST BIOTECH CO., LTD.. The authorized representative in Taiwan is GENERAL BIOLOGICALS CORP..
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