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"Guofa" hemodialysis preparation kit - Taiwan Registration 25ffa3ae8d749045d6a4ec7cf7524c59

Access comprehensive regulatory information for "Guofa" hemodialysis preparation kit in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 25ffa3ae8d749045d6a4ec7cf7524c59 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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25ffa3ae8d749045d6a4ec7cf7524c59
Registration Details
Taiwan FDA Registration: 25ffa3ae8d749045d6a4ec7cf7524c59
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Device Details

"Guofa" hemodialysis preparation kit
TW: "ๅœ‹็™ผ"่ก€ๆถฒ้€ๆžๆบ–ๅ‚™ๅŒ…
Risk Class 2

Registration Details

25ffa3ae8d749045d6a4ec7cf7524c59

DHY00500174205

Company Information

Taiwan, Province of China

Product Details

For details, it is Chinese approved copy of the imitation order

I General, Plastic Surgery and Dermatology

Domestic

Dates and Status

Apr 04, 2006

Apr 04, 2026