Taiwan FDA registration 6dfb9ea085478473ee318ffc07b6dc34
Trinity Biotech V coagulation factor deficiency plasma
TW: 崔尼蒂生技第V凝血因子缺乏血漿
Taiwan·Risk Class 2·TRINITY BIOTECH PLC·Registered May 04, 2006 – May 04, 2011CancelledRegistration details
- Analysis ID
- 6dfb9ea085478473ee318ffc07b6dc34
- Customs Code
- DHA00601654601
Company information
- Manufacturer
- TRINITY BIOTECH PLC
- Manufacturer Country
- Ireland
- Authorized Representative
- BioChain Co., Ltd.
Product details
- Intended Use
- Immunodefactorization was used to quantify the V coagulation factor in human blood.
- Product Type (Level 1)
- B Hematology, pathology, and genetics
- Product Type (Level 2)
- B.7290 factor deficiency test
- Import Information
- import
Dates and status
- Registration Date
- May 04, 2006
- Expiry Date
- May 04, 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 Trinity Biotech V coagulation factor deficiency plasma in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 6dfb9ea085478473ee318ffc07b6dc34 and manufactured by TRINITY BIOTECH PLC. The authorized representative in Taiwan is BioChain Co., Ltd..
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