Taiwan FDA registration a5a4fc1cdf849dfe44ac1d03c811e3a6
Lidelle pregnancy test reagent
TW: 莉黛兒驗孕試劑
Registration details
- Analysis ID
- a5a4fc1cdf849dfe44ac1d03c811e3a6
- Customs Code
- DHY00500204807
Company information
- Manufacturer
- Lianshang Biotechnology Co., Ltd. Wugu Factory
- Manufacturer Country
- Taiwan, Province of China
- Authorized Representative
- PRESIDENT PHARMACEUTICAL CORPORATION
Product details
- Intended Use
- Detection of human placental chorionic gonadal hormone 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
Dates and status
- Registration Date
- May 10, 2006
- Expiry Date
- May 10, 2011
- Cancellation Date
- Nov 01, 2012
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 reagent in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number a5a4fc1cdf849dfe44ac1d03c811e3a6 and manufactured by Lianshang Biotechnology Co., Ltd. Wugu Factory. The authorized representative in Taiwan is PRESIDENT PHARMACEUTICAL CORPORATION.
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