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K.F. Forceps(Sterile) - Taiwan Registration 66ed7696f6b779c62578c47b882cace5

Access comprehensive regulatory information for K.F. Forceps(Sterile) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number 66ed7696f6b779c62578c47b882cace5 and manufactured by Guofa Medical Equipment Co., Ltd. factory. 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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66ed7696f6b779c62578c47b882cace5
Registration Details
Taiwan FDA Registration: 66ed7696f6b779c62578c47b882cace5
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Device Details

K.F. Forceps(Sterile)
TW: ๅœ‹็™ผ้‘ทๅญ(ๆป…่Œ)
Risk Class 1
MD

Registration Details

66ed7696f6b779c62578c47b882cace5

Department of Health Medical Device Manufacturing No. 000373

DHY04300037302

Company Information

Taiwan, Province of China

Product Details

It is a manual instrument for general surgery, a non-powered, hand-held or hand-operated, used and disposable equipment, used for various general surgeries.

I General and plastic surgical devices

I4800 General Surgery Manual Instrument

Produced in Taiwan, China

Dates and Status

Oct 14, 2005

Oct 14, 2025