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Guofa puncture dressing preparation kit - Taiwan Registration 97f65809c7f4938be939a423cb91e3ff

Access comprehensive regulatory information for Guofa puncture dressing 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 97f65809c7f4938be939a423cb91e3ff and manufactured by Guofa Medical Equipment Co., Ltd. factory. 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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97f65809c7f4938be939a423cb91e3ff
Registration Details
Taiwan FDA Registration: 97f65809c7f4938be939a423cb91e3ff
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Device Details

Guofa puncture dressing preparation kit
TW: ๅœ‹็™ผ็ฉฟๅˆบๆ•ทๆ–™ๆบ–ๅ‚™ๅŒ…
Risk Class 2

Registration Details

97f65809c7f4938be939a423cb91e3ff

DHY00500182407

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

Jun 01, 2006

Jun 01, 2026