Taiwan FDA registration 47268b9aad63365a2c74a998a505cbc0

See: Buyani pregnancy test in vitro test card

TW: 瞱成布雅妮驗孕體外測試卡

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

Registration details

Analysis ID: 47268b9aad63365a2c74a998a505cbc0

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: Domestic;; Contract manufacturing

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 See: Buyani 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 47268b9aad63365a2c74a998a505cbc0 and manufactured by Longteng Biotechnology Co., Ltd. The authorized representative in Taiwan is YEA CHANCE ENTERPRISE CO., LTD..

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