Taiwan FDA registration 77c3de629109ee9e4d1bb085ccde27c1
INNO-LiPA HLA-DRB decorder Amplification
TW: 因諾-立帕人類白血球抗原擴增試劑組-DRB位點分析
Taiwan·Risk Class 2·MD·FUJIREBIO EUROPE N.V.·Registered Jul 28, 2015 – Jul 28, 2025CancelledRegistration details
- Analysis ID
- 77c3de629109ee9e4d1bb085ccde27c1
- License Form
- Ministry of Health Medical Device Import No. 027535
- Customs Code
- DHA05602753500
Company information
- Manufacturer
- FUJIREBIO EUROPE N.V.
- Manufacturer Country
- Belgium
- Authorized Representative
- Taiwan Fu Pharmaceutical Co., Ltd
Product details
- Product Type (Level 1)
- B Hematology and pathology devices
- Product Type (Level 2)
- B0001 Human leukocyte antigen segmentation board
- Import Information
- Imported from abroad
Dates and status
- Registration Date
- Jul 28, 2015
- Expiry Date
- Jul 28, 2025
- Cancellation Date
- Oct 28, 2022
Cancellation information
- Status
- Logged out
- Reason
- 公司歇業
About this record
Access comprehensive regulatory information for INNO-LiPA HLA-DRB decorder Amplification in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 77c3de629109ee9e4d1bb085ccde27c1 and manufactured by FUJIREBIO EUROPE N.V.. The authorized representative in Taiwan is Taiwan Fu Pharmaceutical Co., Ltd.
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