Taiwan FDA registration 14f73a1ae716d43e82a2c16bcd3c25a9
"Xindong" pregnancy rapid pregnancy test reagent series (pregnancy test card)
TW: "信東"孕準快速驗孕試劑系列(驗孕卡)
Registration details
- Analysis ID
- 14f73a1ae716d43e82a2c16bcd3c25a9
- Customs Code
- DHY00500310600
Company information
- Manufacturer
- Longteng Biotechnology Co., Ltd
- Manufacturer Country
- Taiwan, Province of China
- Authorized Representative
- TAIWAN BIOTECH CO., LTD.
Product details
- Intended Use
- It is used as a test reagent for early diagnosis of pregnancy.
- Product Type (Level 1)
- A Clinical chemistry and clinical toxicology
- Product Type (Level 2)
- A.1155 Human chorionic gonadotropin testing system
- Import Information
- Contract manufacturing;; Domestic
Dates and status
- Registration Date
- Jul 30, 2010
- Expiry Date
- Feb 09, 2011
- Cancellation Date
- Dec 29, 2011
About this record
Access comprehensive regulatory information for "Xindong" pregnancy rapid pregnancy test reagent series (pregnancy test card) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 14f73a1ae716d43e82a2c16bcd3c25a9 and manufactured by Longteng Biotechnology Co., Ltd. The authorized representative in Taiwan is TAIWAN BIOTECH CO., LTD..
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