Taiwan FDA registration 2be58bffce1614e695dc4a95acc3007b
"Neo-Kehua" Myris human T-lymphotropic virus type 1 and type 2 antibody test reagent
TW: “新科化”妙芮絲人類嗜T淋巴球病毒第一型及第二型抗體檢驗試劑
Taiwan·Risk Class 3·DIASORIN S.P.A. UK BRANCH·Registered Jul 19, 2012 – Aug 12, 2022CancelledRegistration details
- Analysis ID
- 2be58bffce1614e695dc4a95acc3007b
- Customs Code
- DHA00602380707
Company information
- Manufacturer
- DIASORIN S.P.A. UK BRANCH
- Manufacturer Country
- United Kingdom
- Authorized Representative
- NEW SCIENTIFIC EQUIPMENT CO., LTD.
Product details
- Intended Use
- Enzyme immunoassay for human T-lymphophilic virus type I and type II antibodies (HTLV-I and HTLV-II) in human serum or plasma for screening.
- Product Type (Level 1)
- B Hematology, pathology, and genetics
- Product Type (Level 2)
- B.4020 Analysis of specific tests
- Import Information
- import
Dates and status
- Registration Date
- Jul 19, 2012
- Expiry Date
- Aug 12, 2022
- Cancellation Date
- Apr 12, 2024
Cancellation information
- Status
- Logged out
- Reason
- 許可證已逾有效期
About this record
Access comprehensive regulatory information for "Neo-Kehua" Myris human T-lymphotropic virus type 1 and type 2 antibody test reagent in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 3 medical device is registered under number 2be58bffce1614e695dc4a95acc3007b and manufactured by DIASORIN S.P.A. UK BRANCH. The authorized representative in Taiwan is NEW SCIENTIFIC EQUIPMENT CO., LTD..
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