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Hypertherm Respiratory Virus Screening and Identification Kit (Unsterilized) - Taiwan Registration 5f3c2e61e4f82b51a6ba2001dafe98e9

Access comprehensive regulatory information for Hypertherm Respiratory Virus Screening and Identification Kit (Unsterilized) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number 5f3c2e61e4f82b51a6ba2001dafe98e9 and manufactured by DIAGNOSTIC HYBRIDS INCORPORATION. The authorized representative in Taiwan is GLOWAY 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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5f3c2e61e4f82b51a6ba2001dafe98e9
Registration Details
Taiwan FDA Registration: 5f3c2e61e4f82b51a6ba2001dafe98e9
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Device Details

Hypertherm Respiratory Virus Screening and Identification Kit (Unsterilized)
TW: ๆตทๆŸๅ‘ผๅธ้“็—…ๆฏ’็ฏฉ้ธๅ’Œ้‘‘ๅฎš่ฉฆๅŠ‘็ต„(ๆœชๆป…่Œ)
Risk Class 1

Registration Details

5f3c2e61e4f82b51a6ba2001dafe98e9

DHA04400819101

Company Information

United States

Product Details

Limited to the classification and grading management of medical devices, the first level identification range of "respiratory fusion cell virus serum reagent (C.3480)".

C Immunology and microbiology

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

import

Dates and Status

Oct 08, 2009

Oct 08, 2024