Taiwan FDA registration d432c72eb96dbcac02c0418c5c4d4197

Guofa tweezers (sterilized)

TW: 國發鑷子(滅菌)

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

Registration details

Analysis ID: d432c72eb96dbcac02c0418c5c4d4197
Customs Code: DHY04300037302

Company information

Manufacturer: Guofa Medical Equipment Co., Ltd. factory
Manufacturer Country: Taiwan, Province of China
Authorized Representative: K.F. MEDICAL INSTRUMENTS 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, Plastic Surgery and Dermatology
Product Type (Level 2): I.4800 Hand Instruments for General Surgery
Import Information: Domestic

Dates and status

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

About this record

Access comprehensive regulatory information for Guofa tweezers (sterilized) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number d432c72eb96dbcac02c0418c5c4d4197 and manufactured by Guofa Medical Equipment Co., Ltd. factory. The authorized representative in Taiwan is K.F. MEDICAL INSTRUMENTS CO., LTD..

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