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"Guofa" iodine gauze strip - Taiwan Registration 9adbf22257ae685cb60ca0cfc9cda91d

Access comprehensive regulatory information for "Guofa" iodine gauze strip in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 9adbf22257ae685cb60ca0cfc9cda91d 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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9adbf22257ae685cb60ca0cfc9cda91d
Registration Details
Taiwan FDA Registration: 9adbf22257ae685cb60ca0cfc9cda91d
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Device Details

"Guofa" iodine gauze strip
TW: "ๅœ‹็™ผ"ๅ„ช็ข˜็ด—ๅธƒๆข
Risk Class 2

Registration Details

9adbf22257ae685cb60ca0cfc9cda91d

DHY00500174409

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 06, 2006

Apr 06, 2026