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Bioling Influenza A/B Rapid Test Set - Taiwan Registration 30441c1295ffa3b10de205619992e9d3

Access comprehensive regulatory information for Bioling Influenza A/B Rapid Test Set in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number 30441c1295ffa3b10de205619992e9d3 and manufactured by BIOLAND. The authorized representative in Taiwan is PAN EXPAND HEALTH CARE 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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30441c1295ffa3b10de205619992e9d3
Registration Details
Taiwan FDA Registration: 30441c1295ffa3b10de205619992e9d3
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Device Details

Bioling Influenza A/B Rapid Test Set
TW: ็™พๆญ้ˆ A/B ๅž‹ๆตๆ„Ÿๅฟซ้€Ÿๆชข้ฉ—่ฉฆๅŠ‘็ต„
Risk Class 1
Cancelled

Registration Details

30441c1295ffa3b10de205619992e9d3

DHA04400824103

Company Information

Korea, Republic of

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‘

import

Dates and Status

Oct 28, 2009

Oct 28, 2014

Jun 08, 2018

Cancellation Information

Logged out

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