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Americanco A+B influenza virus assay - Taiwan Registration 652c2a5ed2a46fd82669ef578cb5f752

Access comprehensive regulatory information for Americanco A+B influenza virus assay in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number 652c2a5ed2a46fd82669ef578cb5f752 and manufactured by AMERITEK USA. The authorized representative in Taiwan is LIKWANG INSTRUMENTS CO., LTD..

This page provides complete technical specifications, regulatory compliance details. Pure Global AI offers free access to 89,000+ Taiwan medical device registrations, helping global MedTech companies navigate Taiwan FDA regulations, identify competitors, and discover partnership opportunities efficiently.

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652c2a5ed2a46fd82669ef578cb5f752
Registration Details
Taiwan FDA Registration: 652c2a5ed2a46fd82669ef578cb5f752
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Device Details

Americanco A+B influenza virus assay
TW: ไบž็พŽๅˆฉๅฏ A+B ๅž‹ๆต่กŒๆ€งๆ„Ÿๅ†’็—…ๆฏ’ๆชข้ฉ—่ฉฆๅŠ‘
Risk Class 1
Cancelled

Registration Details

652c2a5ed2a46fd82669ef578cb5f752

DHA04600104408

Company Information

China

Product Details

Limited to the first level identification range of the Measures for the Administration of Medical Devices "Influenza Virus Serum Reagent (C.3330)".

C Immunology and microbiology

C.3330 ๆตๆ„Ÿ็—…ๆฏ’่ก€ๆธ…่ฉฆๅŠ‘

Input;; Chinese goods

Dates and Status

Sep 02, 2010

Sep 02, 2020

Jun 22, 2022

Cancellation Information

Logged out

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