Taiwan FDA registration 834ae29ef20b0a157cc00a62a971d377

In vitro reagent for Mingjie pregnancy test

TW: 明傑驗孕體外試劑
Taiwan flagTaiwan·Risk Class 2·Longteng Biotechnology Co., Ltd. Xinshi Factory;; Mingjie Enterprise·Registered Jan 08, 2021 – Oct 26, 2023Expired
Registration details
Analysis ID
834ae29ef20b0a157cc00a62a971d377
Company information
Manufacturer Country
Taiwan, Province of China
Authorized Representative
MIN JIER FIRM
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
國產;; 委託製造;; QMS/QSD
Dates and status
Registration Date
Jan 08, 2021
Expiry Date
Oct 26, 2023
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About this record

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.

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