Taiwan FDA registration 9bd84aa5d787156cf5cb23e528c8450c
Lydelle II Pregnancy Test Series
TW: 莉黛兒Ⅱ驗孕系列
Taiwan·Risk Class 2·Formosa Biomedical Technology Co., Ltd. Yilan Factory·Registered Apr 29, 2010 – Apr 29, 2030ActiveRegistration details
- Analysis ID
- 9bd84aa5d787156cf5cb23e528c8450c
- Customs Code
- DHY00500304009
Company information
- Manufacturer Country
- Taiwan, Province of China
- Authorized Representative
- PRESIDENT PHARMACEUTICAL CORPORATION
Product details
- Intended Use
- This reagent is used by rapid immunochromatography to detect human chorionic gonadotropin (HCG) 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
- Apr 29, 2010
- Expiry Date
- Apr 29, 2030
About this record
Access comprehensive regulatory information for Lydelle II Pregnancy Test Series in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 9bd84aa5d787156cf5cb23e528c8450c and manufactured by Formosa Biomedical Technology Co., Ltd. Yilan Factory. The authorized representative in Taiwan is PRESIDENT PHARMACEUTICAL CORPORATION.
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