Taiwan FDA registration 862d48b5bd4f0a2ec2cf0488e975e392
KatiaTM Chlamydomydia trachomatis IgA antibody detection panel
TW: 卡蒂雅TM沙眼披衣菌IgA抗體檢測試劑組
Taiwan·Risk Class 1·TRINITY BIOTECH USA·Registered Nov 08, 2005 – Nov 08, 2010CancelledRegistration details
- Analysis ID
- 862d48b5bd4f0a2ec2cf0488e975e392
- Customs Code
- DHA04400180705
Company information
- Manufacturer
- TRINITY BIOTECH USA
- Manufacturer Country
- United States
- Authorized Representative
- GRAND MARQUIS CO., LTD.
Product details
- Intended Use
- Detection of antibodies to Chlamydia antigen in human blood.
- Product Type (Level 1)
- C Immunology and microbiology
- Import Information
- import
Dates and status
- Registration Date
- Nov 08, 2005
- Expiry Date
- Nov 08, 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 KatiaTM Chlamydomydia trachomatis IgA antibody detection panel in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number 862d48b5bd4f0a2ec2cf0488e975e392 and manufactured by TRINITY BIOTECH USA. The authorized representative in Taiwan is GRAND MARQUIS CO., LTD..
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