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"Neo-Kehua" Myris human T-lymphotropic virus type 1 and type 2 antibody test reagent - Taiwan Registration 2be58bffce1614e695dc4a95acc3007b

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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2be58bffce1614e695dc4a95acc3007b
Registration Details
Taiwan FDA Registration: 2be58bffce1614e695dc4a95acc3007b
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Device Details

"Neo-Kehua" Myris human T-lymphotropic virus type 1 and type 2 antibody test reagent
TW: โ€œๆ–ฐ็ง‘ๅŒ–โ€ๅฆ™่Šฎ็ตฒไบบ้กžๅ—œTๆท‹ๅทด็ƒ็—…ๆฏ’็ฌฌไธ€ๅž‹ๅŠ็ฌฌไบŒๅž‹ๆŠ—้ซ”ๆชข้ฉ—่ฉฆๅŠ‘
Risk Class 3
Cancelled

Registration Details

2be58bffce1614e695dc4a95acc3007b

DHA00602380707

Company Information

United Kingdom

Product Details

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.

B Hematology, pathology, and genetics

B.4020 Analysis of specific tests

import

Dates and Status

Jul 19, 2012

Aug 12, 2022

Apr 12, 2024

Cancellation Information

Logged out

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