Taiwan FDA registration a61e2a9a862f368b768e3acaa7fd68a1
Pushen triiodothyroxine enzyme immunoassay kit
TW: 普生三碘甲狀腺素酵素免疫分析套組
Taiwan·Risk Class 2·BioCheck, Inc.·Registered Dec 20, 2006 – Dec 20, 2026ActiveRegistration details
- Analysis ID
- a61e2a9a862f368b768e3acaa7fd68a1
- Customs Code
- DHA00601784809
Company information
- Manufacturer
- BioCheck, Inc.
- Manufacturer Country
- United States
- Authorized Representative
- GENERAL BIOLOGICALS CORP.
Product details
- Intended Use
- Quantitative detection of the concentration of triiodothyroxine in human serum.
- Product Type (Level 1)
- A Clinical chemistry and clinical toxicology
- Product Type (Level 2)
- A.1710 Total triiodothyroxine test system
- Import Information
- import
Dates and status
- Registration Date
- Dec 20, 2006
- Expiry Date
- Dec 20, 2026
About this record
Access comprehensive regulatory information for Pushen triiodothyroxine enzyme immunoassay kit in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number a61e2a9a862f368b768e3acaa7fd68a1 and manufactured by BioCheck, Inc.. The authorized representative in Taiwan is GENERAL BIOLOGICALS CORP..
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