Taiwan FDA registration 66ed7696f6b779c62578c47b882cace5

K.F. Forceps(Sterile)

TW: 國發鑷子(滅菌)

Taiwan·Risk Class 1·MD·Guofa Medical Equipment Co., Ltd. factory·Registered Oct 14, 2005 – Oct 14, 2025Expired

Registration details

Analysis ID: 66ed7696f6b779c62578c47b882cace5
License Form: Department of Health Medical Device Manufacturing No. 000373
Customs Code: DHY04300037302

Company information

Manufacturer: Guofa Medical Equipment Co., Ltd. factory
Manufacturer Country: Taiwan, Province of China
Authorized Representative: Guofa Medical Equipment Co., Ltd

Product details

Intended Use: 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.
Product Type (Level 1): I General and plastic surgical devices
Product Type (Level 2): I4800 General Surgery Manual Instrument
Import Information: Produced in Taiwan, China

Dates and status

Registration Date: Oct 14, 2005
Expiry Date: Oct 14, 2025

About this record

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.