Taiwan FDA registration 37b818949e33f0d12ee563db284a371a
In vitro reagents for new human pregnancy tests
TW: 新人類驗孕體外試劑
Taiwan·Risk Class 2·Longteng Biotechnology Co., Ltd. new market factory·Registered Jan 16, 2019 – Jan 16, 2024ExpiredRegistration details
- Analysis ID
- 37b818949e33f0d12ee563db284a371a
Company information
- Manufacturer Country
- Taiwan, Province of China
- Authorized Representative
- JI KON TRADING CO., LTD.
Product details
- Intended Use
- This product qualitatively detects human chorionic gonadotropins in human urine.
- 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
- Jan 16, 2019
- Expiry Date
- Jan 16, 2024
About this record
Access comprehensive regulatory information for In vitro reagents for new human pregnancy tests in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 37b818949e33f0d12ee563db284a371a and manufactured by Longteng Biotechnology Co., Ltd. new market factory. The authorized representative in Taiwan is JI KON TRADING CO., LTD..
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