Taiwan FDA registration e42928a396bd673be75959420b6fb2dd

Lidelle pregnancy test card

TW: 莉黛兒驗孕卡

Taiwan·Risk Class 2·Yongxin Pharmaceutical Industry Co., Ltd. Taichung Lion Factory·Registered Dec 18, 2008 – Dec 18, 2013Cancelled

Registration details

Analysis ID: e42928a396bd673be75959420b6fb2dd
Customs Code: DHY00500271902

Company information

Manufacturer: Yongxin Pharmaceutical Industry Co., Ltd. Taichung Lion Factory
Manufacturer Country: Taiwan, Province of China
Authorized Representative: YUNG SHIN PHARM. IND. CO., LTD.

Product details

Intended Use: The concentration of hCG in human urine is determined.
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: Dec 18, 2008
Expiry Date: Dec 18, 2013
Cancellation Date: Mar 09, 2015

Cancellation information

Status: Logged out
Reason: 許可證已逾有效期

About this record

Access comprehensive regulatory information for Lidelle 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 e42928a396bd673be75959420b6fb2dd and manufactured by Yongxin Pharmaceutical Industry Co., Ltd. Taichung Lion Factory. The authorized representative in Taiwan is YUNG SHIN PHARM. IND. CO., LTD..

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