Taiwan FDA registration ddf3e8d8f107d9ed1c67ff42a74b9dc3
Speedy pregnancy human chorionic gonadotropin test system
TW: 速知孕人類絨毛膜促性腺激素試驗系統
Taiwan·Risk Class 2·IND DIAGNOSTIC INC.·Registered Sep 06, 2005 – Sep 06, 2015CancelledRegistration details
- Analysis ID
- ddf3e8d8f107d9ed1c67ff42a74b9dc3
- Customs Code
- DHA00601222500
Company information
- Manufacturer
- IND DIAGNOSTIC INC.
- Manufacturer Country
- Canada
- Authorized Representative
- SCIENSER INTERNATIONAL INC.
Product details
- Intended Use
- The results of the visual inspection can determine whether you are pregnant.
- Product Type (Level 1)
- A Clinical chemistry and clinical toxicology
- Import Information
- import
Dates and status
- Registration Date
- Sep 06, 2005
- Expiry Date
- Sep 06, 2015
- Cancellation Date
- Aug 09, 2018
Cancellation information
- Status
- Logged out
- Reason
- 未展延而逾期者
About this record
Access comprehensive regulatory information for Speedy pregnancy human chorionic gonadotropin test system in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number ddf3e8d8f107d9ed1c67ff42a74b9dc3 and manufactured by IND DIAGNOSTIC INC.. The authorized representative in Taiwan is SCIENSER INTERNATIONAL INC..
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