In vitro reagent for Mingjie pregnancy test
- Analysis ID
- 834ae29ef20b0a157cc00a62a971d377
- Manufacturer Country
- Taiwan, Province of China
- Authorized Representative
- MIN JIER FIRM
- 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
- 國產;; 委託製造;; QMS/QSD
- Registration Date
- Jan 08, 2021
- Expiry Date
- Oct 26, 2023
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Access comprehensive regulatory information for In vitro reagent for Mingjie 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 834ae29ef20b0a157cc00a62a971d377 and manufactured by Longteng Biotechnology Co., Ltd. Xinshi Factory;; Mingjie Enterprise. The authorized representative in Taiwan is MIN JIER FIRM.
This page provides complete technical specifications, regulatory compliance details, 1 companies making similar products including Longteng Biotechnology Co., Ltd. Xinshi Factory;; Mingjie Enterprise, and 1 recent registrations in the same category. Pure Global AI offers free access to 89,000+ Taiwan medical device registrations, helping global MedTech companies navigate Taiwan FDA regulations, identify competitors, and discover partnership opportunities efficiently.