Taiwan FDA registration 1dc904fa2666520f2a81aaa9e9660e7f
Baby Pregnancy Test II Test Reagent
TW: 葳兒驗孕卡 II 檢驗試劑
Taiwan·Risk Class 2·SYNTRON BIORESEARCH, INC.·Registered Nov 19, 2007 – Nov 19, 2012CancelledRegistration details
- Analysis ID
- 1dc904fa2666520f2a81aaa9e9660e7f
- Customs Code
- DHA00601868104
Company information
- Manufacturer
- SYNTRON BIORESEARCH, INC.
- Manufacturer Country
- United States
- Authorized Representative
- WELLDENG INTERNATIONAL CO., LTD.
Product details
- Intended Use
- Immunochromatography was used to qualitatively detect 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
- import
Dates and status
- Registration Date
- Nov 19, 2007
- Expiry Date
- Nov 19, 2012
- Cancellation Date
- Apr 30, 2014
Cancellation information
- Status
- Logged out
- Reason
- 許可證已逾有效期
About this record
Access comprehensive regulatory information for Baby Pregnancy Test II 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 1dc904fa2666520f2a81aaa9e9660e7f and manufactured by SYNTRON BIORESEARCH, INC.. The authorized representative in Taiwan is WELLDENG INTERNATIONAL CO., LTD..
This page provides complete technical specifications, regulatory compliance details. Pure Global AI offers free access to 89,000+ Taiwan medical device registrations, helping global MedTech companies navigate Taiwan FDA regulations, identify competitors, and discover partnership opportunities efficiently.
Free DatabasePowered by Pure Global AI89,000+ Devices