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Wonderford Influenza A/B Virus Rapid Test Reagent (Unsterilized) - Taiwan Registration b198b5a0155a0c480b3d139d7621aa91

Access comprehensive regulatory information for Wonderford Influenza A/B Virus Rapid Test Reagent (Unsterilized) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number b198b5a0155a0c480b3d139d7621aa91 and manufactured by WONDFO BIOTECH CO., LTD. The authorized representative in Taiwan is GENERAL BIOLOGICALS 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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b198b5a0155a0c480b3d139d7621aa91
Registration Details
Taiwan FDA Registration: b198b5a0155a0c480b3d139d7621aa91
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Device Details

Wonderford Influenza A/B Virus Rapid Test Reagent (Unsterilized)
TW: ่ฌๅพท็ฆA/Bๅž‹ๆตๆ„Ÿ็—…ๆฏ’ๅฟซ้€Ÿๆชขๆธฌ่ฉฆๅŠ‘(ๆœชๆป…่Œ)
Risk Class 1

Registration Details

b198b5a0155a0c480b3d139d7621aa91

DHA04600080308

Company Information

China

Product Details

It is limited to the first-level identification scope of influenza virus serum reagent (C.3330) in the classification and grading management measures for medical devices.

C Immunology and microbiology

C.3330 ๆตๆ„Ÿ็—…ๆฏ’่ก€ๆธ…่ฉฆๅŠ‘

Chinese goods;; input

Dates and Status

Sep 30, 2009

Sep 30, 2024