Taiwan FDA registration be856a58c6225cba8392dd8e6bdc9ec4

Eugene pregnancy test card

TW: 優來驗孕卡
Taiwan flagTaiwan·Risk Class 2·Longteng Biotechnology Co., Ltd·Registered Nov 05, 2013 – Feb 09, 2016Cancelled
Registration details
Analysis ID
be856a58c6225cba8392dd8e6bdc9ec4
Company information
Manufacturer Country
Taiwan, Province of China
Authorized Representative
U-LIANG PHARMACEUTICAL CO., LTD.
Product details
Intended Use
It is used as a test reagent for early diagnosis of pregnancy.
Product Type (Level 1)
A Clinical chemistry and clinical toxicology
Product Type (Level 2)
A.1155 Human chorionic gonadotropin testing system
Import Information
Contract manufacturing;; Domestic
Dates and status
Registration Date
Nov 05, 2013
Expiry Date
Feb 09, 2016
Cancellation Date
Nov 17, 2017
Cancellation information
Status
Logged out
Reason
自請註銷;;未展延而逾期者
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About this record

Access comprehensive regulatory information for Eugene pregnancy test card in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number be856a58c6225cba8392dd8e6bdc9ec4 and manufactured by Longteng Biotechnology Co., Ltd. The authorized representative in Taiwan is U-LIANG PHARMACEUTICAL CO., LTD..

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