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"Remeng" Wicker * Neisseria meningococcus B / E. coli K1 test kit - Taiwan Registration 83d8bf74a3bebd20fd2210a954ff25d2

Access comprehensive regulatory information for "Remeng" Wicker * Neisseria meningococcus B / E. coli K1 test kit in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 83d8bf74a3bebd20fd2210a954ff25d2 and manufactured by REMEL EUROPE LIMITED. The authorized representative in Taiwan is SCN TRADING COMPANY LIMITED.

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83d8bf74a3bebd20fd2210a954ff25d2
Registration Details
Taiwan FDA Registration: 83d8bf74a3bebd20fd2210a954ff25d2
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Device Details

"Remeng" Wicker * Neisseria meningococcus B / E. coli K1 test kit
TW: ใ€้Šณ็›Ÿใ€žๅจๅ…‹่Œ*ๅฅˆ็‘Ÿๆฐ่…ฆ่†œ็‚Ž็ƒ่Œ B ็พค/ๅคง่…ธๆกฟ่ŒK1ๅž‹ๆชขๆธฌๅฅ—็ต„
Risk Class 2
Cancelled

Registration Details

83d8bf74a3bebd20fd2210a954ff25d2

DHA00601530908

Company Information

United Kingdom

Product Details

A rapid latex assay for the qualitative detection of antigens of Neisseri's meningitis (meningococcal) group B and E. coli K1 in body fluids or blood culture supernatants as a result of infection.

C Immunology and microbiology

C.3390 ๅฅˆ็‘Ÿๆฐ่Œๅฑฌ็›ดๆŽฅ่ก€ๆธ…่ฉฆๅŠ‘

import

Dates and Status

Dec 07, 2005

Dec 07, 2015

May 17, 2018

Cancellation Information

Logged out

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