Taiwan FDA registration f733ed19ef7bf33725bb1144dff833c2
INNO-LIA HTLV I/II Score
TW: 因諾-立亞人類嗜T淋巴球病毒第一/二型在線免疫分析試劑組
Taiwan·Risk Class 3·MD·FUJIREBIO EUROPE N.V.·Registered Feb 04, 2020 – Feb 04, 2025CancelledRegistration details
- Analysis ID
- f733ed19ef7bf33725bb1144dff833c2
- License Form
- Ministry of Health Medical Device Import No. 033262
- Customs Code
- DHA05603326203
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)
- B4020 Analyze specific reagents
- Import Information
- Imported from abroad
Dates and status
- Registration Date
- Feb 04, 2020
- Expiry Date
- Feb 04, 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-LIA HTLV I/II Score in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 3 medical device is registered under number f733ed19ef7bf33725bb1144dff833c2 and manufactured by FUJIREBIO EUROPE N.V.. The authorized representative in Taiwan is Taiwan Fu Pharmaceutical Co., Ltd.
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