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Lenus Respiratory Virus Nucleic Acid Test Reagent (2nd Generation) - Taiwan Registration d5321f53ca885888c1a8cb147b955655

Access comprehensive regulatory information for Lenus Respiratory Virus Nucleic Acid Test Reagent (2nd Generation) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number d5321f53ca885888c1a8cb147b955655 and manufactured by LUMINEX MOLECULAR DIAGNOSTICS, INC.. The authorized representative in Taiwan is REFERENCE TECHNOLOGY LIMITED COMPANY.

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d5321f53ca885888c1a8cb147b955655
Registration Details
Taiwan FDA Registration: d5321f53ca885888c1a8cb147b955655
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Device Details

Lenus Respiratory Virus Nucleic Acid Test Reagent (2nd Generation)
TW: ๅ€ซ็ดๆ–ฏๅ‘ผๅธ้“็—…ๆฏ’ๆ ธ้…ธๆชข้ฉ—่ฉฆๅŠ‘(็ฌฌไบŒไปฃ)
Risk Class 2
Cancelled

Registration Details

d5321f53ca885888c1a8cb147b955655

DHA05602806102

Company Information

Product Details

This product is a multiplex nucleic acid qualitative test reagent, which is used for nasopharyngeal sampling swabs, nasal aspirates or bronchoalveolar lavage fluid of individuals suspected of respiratory tract infection, and simultaneously detects and identifies a variety of respiratory viral nucleic acids.

C Immunology and microbiology

C.3980 ๅ‘ผๅธ้“็—…ๆฏ’ๅคšๆจ™็š„ๆ ธ้…ธๆชข้ฉ—่ฉฆๅŠ‘

import

Dates and Status

Dec 25, 2015

Dec 25, 2020

Jun 17, 2022

Cancellation Information

Logged out

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