Taiwan FDA registration 14e57ac751a197691b15af3a391061e1

Cheng Fangting pregnancy test in vitro test pen

TW: 瞱成芳婷驗孕體外測試筆

Taiwan·Risk Class 2·Longteng Biotechnology Co., Ltd·Registered Apr 10, 2013 – Dec 12, 2015Cancelled

Registration details

Analysis ID: 14e57ac751a197691b15af3a391061e1

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: Dec 12, 2015
Cancellation Date: Jun 26, 2018

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 pen in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 14e57ac751a197691b15af3a391061e1 and manufactured by Longteng Biotechnology Co., Ltd. The authorized representative in Taiwan is YEA CHANCE ENTERPRISE CO., LTD..

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