Taiwan FDA registration 7be06c784b64c8778224f50a0c1e729e
Trinity Biotech IX coagulation factor deficiency plasma
TW: 崔尼蒂生技第IX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
- 7be06c784b64c8778224f50a0c1e729e
- Customs Code
- DHA00601654502
Company information
- Manufacturer
- TRINITY BIOTECH PLC
- Manufacturer Country
- Ireland
- Authorized Representative
- BioChain Co., Ltd.
Product details
- Intended Use
- Immunocytokine IX was quantified by coagulation method in human plasma.
- 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 IX 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 7be06c784b64c8778224f50a0c1e729e and manufactured by TRINITY BIOTECH PLC. The authorized representative in Taiwan is BioChain Co., Ltd..
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