Taiwan FDA registration 7de2bc6fdcb3ca0100d3752664935426
Armas Automated D Duplex Test Set
TW: 阿瑪斯自動D雙體檢驗試劑組
Taiwan·Risk Class 2·TRINITY BIOTECH PLC·Registered Nov 22, 2006 – Nov 22, 2011CancelledRegistration details
- Analysis ID
- 7de2bc6fdcb3ca0100d3752664935426
- Customs Code
- DHA00601761206
Company information
- Manufacturer
- TRINITY BIOTECH PLC
- Manufacturer Country
- Ireland
- Authorized Representative
- BioChain Co., Ltd.
Product details
- Intended Use
- Quantification of fibrin schizome products containing D-dimers in human plasma using an automated coagulation analyzer.
- Product Type (Level 1)
- B Hematology, pathology, and genetics
- Product Type (Level 2)
- B.7320 Fibrinogen/Fibrinolysis Product Analysis
- Import Information
- import
Dates and status
- Registration Date
- Nov 22, 2006
- Expiry Date
- Nov 22, 2011
- Cancellation Date
- Nov 09, 2012
Cancellation information
- Status
- Logged out
- Reason
- 許可證已逾有效期
About this record
Access comprehensive regulatory information for Armas Automated D Duplex 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 7de2bc6fdcb3ca0100d3752664935426 and manufactured by TRINITY BIOTECH PLC. The authorized representative in Taiwan is BioChain Co., Ltd..
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