Taiwan FDA registration 0e804f0e55d68b40e4ed8e4c63f6473a
Pursen rapid visual analysis group of human chorionic gonadotropin enzyme immunoassays
TW: 普生快速目測式的人類絨毛膜促性腺激素酵素免疫分析組
Taiwan·Risk Class 2·BIOCHECK, INC.·Registered Dec 13, 2006 – Dec 13, 2016CancelledRegistration details
- Analysis ID
- 0e804f0e55d68b40e4ed8e4c63f6473a
- Customs Code
- DHA00601783003
Company information
- Manufacturer
- BIOCHECK, INC.
- Manufacturer Country
- United States
- Authorized Representative
- GENERAL BIOLOGICALS CORP.
Product details
- Intended Use
- Qualitative or quantitative analysis of human chorionic gonadotropin (hCG) in urine or serum is indicated.
- 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
- Dec 13, 2006
- Expiry Date
- Dec 13, 2016
- Cancellation Date
- Jun 28, 2018
Cancellation information
- Status
- Logged out
- Reason
- 許可證已逾有效期
About this record
Access comprehensive regulatory information for Pursen rapid visual analysis group of human chorionic gonadotropin enzyme immunoassays in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 0e804f0e55d68b40e4ed8e4c63f6473a and manufactured by BIOCHECK, INC.. The authorized representative in Taiwan is GENERAL BIOLOGICALS CORP..
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