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"K.F." CURING SHEET - Taiwan Registration 68687ead60f4dda28981be690fceb6a2

Access comprehensive regulatory information for "K.F." CURING SHEET in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 68687ead60f4dda28981be690fceb6a2 and manufactured by K.F. MEDICAL INSTRUMENTS CO., LTD.. The authorized representative in Taiwan is Guofa Medical Equipment 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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68687ead60f4dda28981be690fceb6a2
Registration Details
Taiwan FDA Registration: 68687ead60f4dda28981be690fceb6a2
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Device Details

"K.F." CURING SHEET
TW: "ๅœ‹็™ผ"ๆฒป็™‚ๅทพ
Risk Class 2
MD

Registration Details

68687ead60f4dda28981be690fceb6a2

Department of Health Medical Device Manufacturing No. 001737

DHY00500173702

Company Information

Taiwan, Province of China

Product Details

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

I General and plastic surgical devices

Produced in Taiwan, China

Dates and Status

Apr 03, 2006

Apr 03, 2026