Buyani pregnancy test in vitro test
- Analysis ID
- f44fb1776a9ac50170c37cbd15f48630
- Manufacturer
- Longteng Biotechnology Co., Ltd
- Manufacturer Country
- Taiwan, Province of China
- Authorized Representative
- YEA CHANCE ENTERPRISE CO., LTD.
- 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
- Registration Date
- Apr 09, 2013
- Expiry Date
- Dec 12, 2015
- Cancellation Date
- Jun 26, 2018
- Status
- Logged out
- Reason
- 許可證已逾有效期
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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.