Taiwan FDA registration 374ec6194e276cf7d0081f0f4b182cdf
KatiaTM thyroglobulin antibody test set
TW: 卡蒂雅TM甲狀腺球蛋白抗體檢測試劑組
Registration details
- Analysis ID
- 374ec6194e276cf7d0081f0f4b182cdf
- Customs Code
- DHA00601727300
Company information
- Manufacturer
- TRINITY BIOTECH USA
- Manufacturer Country
- United States
- Authorized Representative
- GRAND MARQUIS CO., LTD.
Product details
- Intended Use
- Enzyme immunoadsorption assay was used to detect thyroglobulin antibody in human serum.
- Product Type (Level 1)
- A Clinical chemistry and clinical toxicology
- Product Type (Level 2)
- A.1685 Thyroxine-binding globulin testing system
- Import Information
- import
Dates and status
- Registration Date
- Aug 10, 2006
- Expiry Date
- Aug 10, 2011
- Cancellation Date
- Nov 27, 2012
Cancellation information
- Status
- Logged out
- Reason
- 許可證已逾有效期
About this record
Access comprehensive regulatory information for KatiaTM thyroglobulin antibody test set in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 374ec6194e276cf7d0081f0f4b182cdf and manufactured by TRINITY BIOTECH USA. The authorized representative in Taiwan is GRAND MARQUIS CO., LTD..
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