Taiwan FDA registration e6971d7a483afba1ab788cc9aece89aa
ULIP Rapid Pregnancy Test Reagent
TW: 優立盼 快速驗孕試劑
Registration details
- Analysis ID
- e6971d7a483afba1ab788cc9aece89aa
Company information
- Manufacturer Country
- Taiwan, Province of China
- Authorized Representative
- Minsong Industrial Co., Ltd
Product details
- Intended Use
- The urine is tested qualitatively for human chorionic gonadotropin. New performance: Added non-professional use.
- Product Type (Level 1)
- A Clinical chemistry and clinical toxicology
- Product Type (Level 2)
- A.1155 Human chorionic gonadotropin testing system
- Import Information
- Domestic;; Contract manufacturing
Dates and status
- Registration Date
- May 01, 2017
- Expiry Date
- Sep 28, 2025
About this record
Access comprehensive regulatory information for ULIP 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 e6971d7a483afba1ab788cc9aece89aa and manufactured by Minsong Industrial Co., Ltd.;; Dongyao Biotechnology Co., Ltd. The authorized representative in Taiwan is Minsong Industrial Co., Ltd.
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