Taiwan FDA registration 79d2261984e81f04c8843676c6f5d026
GB hCG EIA Kit
TW: 普生人類絨毛膜促性腺激素酵素免疫分析套組
Taiwan·Risk Class 2·MD·BioCheck, Inc.·Registered Sep 22, 2014 – Sep 22, 2024CancelledRegistration details
- Analysis ID
- 79d2261984e81f04c8843676c6f5d026
- License Form
- Ministry of Health Medical Device Import No. 026535
- Customs Code
- DHA05602653508
Company information
- Manufacturer
- BioCheck, Inc.
- Manufacturer Country
- United States
- Authorized Representative
- GENERAL BIOLOGICALS CORP.
Product details
- Product Type (Level 1)
- A Clinical chemistry and clinical toxicology
- Product Type (Level 2)
- A1155 Human chorionic gonadotropin test system
- Import Information
- Imported from abroad
Dates and status
- Registration Date
- Sep 22, 2014
- Expiry Date
- Sep 22, 2024
- Cancellation Date
- May 17, 2023
Cancellation information
- Status
- Logged out
- Reason
- 自請註銷
About this record
Access comprehensive regulatory information for GB hCG EIA Kit in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 79d2261984e81f04c8843676c6f5d026 and manufactured by BioCheck, Inc.. The authorized representative in Taiwan is GENERAL BIOLOGICALS CORP..
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