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"Neoscienceization" Myorest Human Immunodeficiency Virus Antibody Reagent - Taiwan Registration bbffe771c150f6a154cedd8a562bd0b9

Access comprehensive regulatory information for "Neoscienceization" Myorest Human Immunodeficiency Virus Antibody Reagent in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 3 medical device is registered under number bbffe771c150f6a154cedd8a562bd0b9 and manufactured by DIASORIN S.P.A. UK BRANCH. The authorized representative in Taiwan is NEW SCIENTIFIC EQUIPMENT CO., LTD..

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bbffe771c150f6a154cedd8a562bd0b9
Registration Details
Taiwan FDA Registration: bbffe771c150f6a154cedd8a562bd0b9
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Device Details

"Neoscienceization" Myorest Human Immunodeficiency Virus Antibody Reagent
TW: โ€œๆ–ฐ็ง‘ๅŒ–โ€ ๅฆ™่Šฎ็ตฒไบบ้กžๅ…็–ซ็ผบไน็—…ๆฏ’ๆŠ—้ซ”่ฉฆๅŠ‘
Risk Class 3
Cancelled

Registration Details

bbffe771c150f6a154cedd8a562bd0b9

DHA00602380302

Company Information

United Kingdom

Product Details

Enzyme immunoassay for statutory testing of human immunodeficiency virus type 1 (HIV-1, HIV-1O subtype) and type II (HIV-2) antibodies in human serum or plasma for screening.

B Hematology, pathology, and genetics

B.4020 Analysis of specific tests

import

Dates and Status

Jul 16, 2012

Aug 08, 2022

Apr 12, 2024

Cancellation Information

Logged out

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