Taiwan FDA registration f44fb1776a9ac50170c37cbd15f48630

Buyani pregnancy test in vitro test

TW: 瞱成布雅妮驗孕體外測試筆
Taiwan flagTaiwan·Risk Class 2·Longteng Biotechnology Co., Ltd·Registered Apr 09, 2013 – Dec 12, 2015Cancelled
Registration details
Analysis ID
f44fb1776a9ac50170c37cbd15f48630
Company information
Manufacturer Country
Taiwan, Province of China
Authorized Representative
YEA CHANCE ENTERPRISE CO., LTD.
Product details
Intended Use
Qualitative detection of human chorionic gonadotropin in urine.
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
Apr 09, 2013
Expiry Date
Dec 12, 2015
Cancellation Date
Jun 26, 2018
Cancellation information
Status
Logged out
Reason
許可證已逾有效期
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About this record

Access comprehensive regulatory information for Buyani pregnancy test in vitro test in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number f44fb1776a9ac50170c37cbd15f48630 and manufactured by Longteng Biotechnology Co., Ltd. The authorized representative in Taiwan is YEA CHANCE ENTERPRISE CO., LTD..

This page provides complete technical specifications, regulatory compliance details, 1 companies making similar products including Longteng Biotechnology Co., Ltd, and 2 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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