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In vitro reagent for Mingjie pregnancy test - Taiwan Registration 834ae29ef20b0a157cc00a62a971d377

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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834ae29ef20b0a157cc00a62a971d377
Registration Details
Taiwan FDA Registration: 834ae29ef20b0a157cc00a62a971d377
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Device Details

In vitro reagent for Mingjie pregnancy test
TW: ๆ˜Žๅ‚‘้ฉ—ๅญ•้ซ”ๅค–่ฉฆๅŠ‘
Risk Class 2

Registration Details

834ae29ef20b0a157cc00a62a971d377

Company Information

Product Details

This product qualitatively detects human chorionic gonadotropins in human urine.

A Clinical chemistry and clinical toxicology

A.1155 Human chorionic gonadotropin testing system

ๅœ‹็”ข;; ๅง”่จ—่ฃฝ้€ ;; QMS/QSD

Dates and Status

Jan 08, 2021

Oct 26, 2023

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