Taiwan FDA registration 16e658ebe6d9a0ebfdbef614c7425962
Katia Helicobacter pylori IgA antibody detection kit
TW: 卡蒂雅幽門螺旋桿菌IgA抗體檢測試劑組
Taiwan·Risk Class 1·TRINITY BIOTECH USA·Registered Nov 07, 2005 – Nov 07, 2010CancelledRegistration details
- Analysis ID
- 16e658ebe6d9a0ebfdbef614c7425962
- Customs Code
- DHA04400179103
Company information
- Manufacturer
- TRINITY BIOTECH USA
- Manufacturer Country
- United States
- Authorized Representative
- GRAND MARQUIS CO., LTD.
Product details
- Intended Use
- Detection of IgA antibodies to Helicobacter pylori in human serum.
- Product Type (Level 1)
- C Immunology and microbiology
- Import Information
- import
Dates and status
- Registration Date
- Nov 07, 2005
- Expiry Date
- Nov 07, 2010
- 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 Katia Helicobacter pylori IgA antibody detection kit in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number 16e658ebe6d9a0ebfdbef614c7425962 and manufactured by TRINITY BIOTECH USA. The authorized representative in Taiwan is GRAND MARQUIS CO., LTD..
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