Taiwan FDA registration e64e06d2d23e9603b7a80cde375220a4

Eugene pregnancy test card

TW: 優來 驗孕卡
Taiwan flagTaiwan·Risk Class 2·Longteng Biotechnology Co., Ltd·Registered Oct 11, 2007 – Oct 11, 2012Cancelled
Registration details
Analysis ID
e64e06d2d23e9603b7a80cde375220a4
Customs Code
DHY00500246803
Company information
Manufacturer Country
Taiwan, Province of China
Authorized Representative
U-LIANG PHARMACEUTICAL CO., LTD.
Product details
Intended Use
Qualitative testing of human pilionic gonadotropins.
Product Type (Level 1)
A Clinical chemistry and clinical toxicology
Product Type (Level 2)
A.1155 Human chorionic gonadotropin testing system
Import Information
Domestic
Dates and status
Registration Date
Oct 11, 2007
Expiry Date
Oct 11, 2012
Cancellation Date
Apr 03, 2014
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 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 e64e06d2d23e9603b7a80cde375220a4 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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