Taiwan FDA registration 61868cb07ccd24794010a190420f45eb
Keffer rapid pregnancy test reagent
TW: 凱富快速驗孕檢驗試劑
Taiwan·Risk Class 2·HANGZHOU BIOTEST BIOTECH CO., LTD.·Registered Dec 12, 2014 – Dec 12, 2029ActiveRegistration details
- Analysis ID
- 61868cb07ccd24794010a190420f45eb
- Customs Code
- DHA09200066101
Company information
- Manufacturer
- HANGZHOU BIOTEST BIOTECH CO., LTD.
- Manufacturer Country
- China
- Authorized Representative
- K&G ENTERPRISE CO., LTD. TAIWAN BRANCH (BVI)
Product details
- Intended Use
- This product uses rapid immunochromatography to detect human chorionic gonadotropin (HCG) in the sample to detect pregnancy early.
- Product Type (Level 1)
- A Clinical chemistry and clinical toxicology
- Product Type (Level 2)
- A.1155 Human chorionic gonadotropin testing system
- Import Information
- Input;; Chinese goods
Dates and status
- Registration Date
- Dec 12, 2014
- Expiry Date
- Dec 12, 2029
About this record
Access comprehensive regulatory information for Keffer rapid pregnancy test reagent in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 61868cb07ccd24794010a190420f45eb and manufactured by HANGZHOU BIOTEST BIOTECH CO., LTD.. The authorized representative in Taiwan is K&G ENTERPRISE CO., LTD. TAIWAN BRANCH (BVI).
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