Taiwan FDA registration 1141e70a9cb133a5f33749061150c383
"Amity" rapid pregnancy test
TW: “愛德” 快速驗孕試劑
Taiwan·Risk Class 2·AIDE Diagnostic Co., Ltd·Registered Apr 22, 2015 – Apr 22, 2025ExpiredRegistration details
- Analysis ID
- 1141e70a9cb133a5f33749061150c383
- Customs Code
- DHA09200066509
Company information
- Manufacturer
- AIDE Diagnostic Co., Ltd
- Manufacturer Country
- China
- Authorized Representative
- SCIENSER INTERNATIONAL INC.
Product details
- Intended Use
- It is used to qualitatively detect human chorionic gonadotropin (HCG) in women's urine to provide a basis for early pregnancy diagnosis.
- Product Type (Level 1)
- A Clinical chemistry and clinical toxicology
- Product Type (Level 2)
- A.1155 Human chorionic gonadotropin testing system
- Import Information
- Input;; Chinese goods
Dates and status
- Registration Date
- Apr 22, 2015
- Expiry Date
- Apr 22, 2025
About this record
Access comprehensive regulatory information for "Amity" rapid pregnancy test in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 1141e70a9cb133a5f33749061150c383 and manufactured by AIDE Diagnostic Co., Ltd. The authorized representative in Taiwan is SCIENSER INTERNATIONAL INC..
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