Taiwan FDA registration ca31e9fce099b02779f30e5ba59637f9

Cheng Fangting pregnancy test in vitro test card

TW: 瞱成芳婷驗孕體外測試卡

Taiwan·Risk Class 2·Longteng Biotechnology Co., Ltd·Registered Apr 10, 2013 – Feb 09, 2016Cancelled

Registration details

Analysis ID: ca31e9fce099b02779f30e5ba59637f9

Company information

Manufacturer: Longteng Biotechnology Co., Ltd
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: Contract manufacturing;; Domestic

Dates and status

Registration Date: Apr 10, 2013
Expiry Date: Feb 09, 2016
Cancellation Date: May 13, 2016

Cancellation information

Status: Logged out
Reason: 許可證已逾有效期

About this record

Access comprehensive regulatory information for Cheng Fangting pregnancy test in vitro 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 ca31e9fce099b02779f30e5ba59637f9 and manufactured by Longteng Biotechnology Co., Ltd. The authorized representative in Taiwan is YEA CHANCE ENTERPRISE CO., LTD..

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