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Guofa Smear Kit (Unsterilized) - Taiwan Registration a7a9723e6d1d049d29b9a2ffc0c9dabd

Access comprehensive regulatory information for Guofa Smear 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 a7a9723e6d1d049d29b9a2ffc0c9dabd and manufactured by K.F. MEDICAL INSTRUMENTS CO., LTD.. The authorized representative in Taiwan is K.F. MEDICAL INSTRUMENTS 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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a7a9723e6d1d049d29b9a2ffc0c9dabd
Registration Details
Taiwan FDA Registration: a7a9723e6d1d049d29b9a2ffc0c9dabd
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Device Details

Guofa Smear Kit (Unsterilized)
TW: ๅœ‹็™ผๆŠน็‰‡็ต„ๅˆๅŒ…(ๆœชๆป…่Œ)
Risk Class 1

Registration Details

a7a9723e6d1d049d29b9a2ffc0c9dabd

DHY04300130809

Company Information

Taiwan, Province of China

Product Details

C Immunology and microbiology

C.2900 Microbial sample collection and delivery equipment

Domestic

Dates and Status

Apr 21, 2006

Apr 21, 2026