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Respiratory Fusion Virus Rapid Test (Unsterilized) - Taiwan Registration 0577302791e1d7c13e37dc8ea2b4c475

Access comprehensive regulatory information for Respiratory Fusion Virus Rapid Test (Unsterilized) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number 0577302791e1d7c13e37dc8ea2b4c475 and manufactured by VEDA LAB. The authorized representative in Taiwan is RAFA INTERNATIONAL CORP..

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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0577302791e1d7c13e37dc8ea2b4c475
Registration Details
Taiwan FDA Registration: 0577302791e1d7c13e37dc8ea2b4c475
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Device Details

Respiratory Fusion Virus Rapid Test (Unsterilized)
TW: ๅง”้”ๅ‘ผๅธ้“่žๅˆ็—…ๆฏ’ๅฟซ้€Ÿๆชขๆธฌ็‰‡(ๆœชๆป…่Œ)
Risk Class 1

Registration Details

0577302791e1d7c13e37dc8ea2b4c475

DHA04400089408

Company Information

France

Product Details

Detection of respiratory cell fusion virus (RSV) using the principle of immunochromatography.

C Immunology and microbiology

C.3480 ๅ‘ผๅธ้“่žๅˆ็ดฐ่ƒž็—…ๆฏ’่ก€ๆธ…่ฉฆๅŠ‘

import

Dates and Status

Oct 12, 2005

Oct 12, 2025