Taiwan FDA registration 2987c0d963769526e347b99e121fdfc1
New Love Rapid Pregnancy Test Reagent
TW: 新情 快速驗孕試劑
Registration details
- Analysis ID
- 2987c0d963769526e347b99e121fdfc1
Company information
- Manufacturer Country
- Taiwan, Province of China
- Authorized Representative
- Liguo Pharmaceutical Co., Ltd
Product details
- Intended Use
- Urine is tested qualitatively for human chorionic gonadotropin (HCG).
- 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
- May 01, 2017
- Expiry Date
- Sep 28, 2025
About this record
Access comprehensive regulatory information for New Love 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 2987c0d963769526e347b99e121fdfc1 and manufactured by Dongyao Biotechnology Co., Ltd.;; Liguo Pharmaceutical Co., Ltd. The authorized representative in Taiwan is Liguo Pharmaceutical Co., Ltd.
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