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"Dirk" enterovirus antigen enzyme immunoassay group - Taiwan Registration 40a49a1b4833ccf00938eb1b258ae5e5

Access comprehensive regulatory information for "Dirk" enterovirus antigen enzyme immunoassay group in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number 40a49a1b4833ccf00938eb1b258ae5e5 and manufactured by Baoling Fujin Biotechnology Co., Ltd. Medical Equipment Factory. The authorized representative in Taiwan is Dirk International Limited.

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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40a49a1b4833ccf00938eb1b258ae5e5
Registration Details
Taiwan FDA Registration: 40a49a1b4833ccf00938eb1b258ae5e5
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Device Details

"Dirk" enterovirus antigen enzyme immunoassay group
TW: "ๅพทๅ…‹" ่…ธ็—…ๆฏ’ๆŠ—ๅŽŸ้…ต็ด ๅ…็–ซ่ฉฆๅŠ‘็ต„
Risk Class 1
Cancelled

Registration Details

40a49a1b4833ccf00938eb1b258ae5e5

DHY04300171002

Company Information

Product Details

Limited to the first level identification range of the Measures for the Administration of Medical Devices "Koshaki Virus Serum Reagent (C.3145)".

C Immunology and microbiology

C.3145 ๆŸฏๆฒ™ๅฅ‡็—…ๆฏ’่ก€ๆธ…่ฉฆๅŠ‘

Domestic;; Contract manufacturing

Dates and Status

Nov 21, 2006

Nov 21, 2011

Nov 16, 2012

Cancellation Information

Logged out

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