Taiwan FDA registration 154f9a5dee96b6972a2ea7e7e397c5b7
In vitro reagent for the pregnancy test
TW: 優立盼驗孕體外試劑
Registration details
- Analysis ID
- 154f9a5dee96b6972a2ea7e7e397c5b7
Company information
- Manufacturer Country
- Taiwan, Province of China
- Authorized Representative
- Minsong Industrial 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
- Apr 22, 2019
- Expiry Date
- Oct 26, 2023
About this record
Access comprehensive regulatory information for In vitro reagent for the pregnancy test in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 154f9a5dee96b6972a2ea7e7e397c5b7 and manufactured by Minsong Industrial Co., Ltd.;; Longteng Biotech Co., Ltd. Xinshi Plant. The authorized representative in Taiwan is Minsong Industrial Co., Ltd.
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