Taiwan FDA registration 9adbf22257ae685cb60ca0cfc9cda91d

"Guofa" iodine gauze strip

TW: "國發"優碘紗布條

Taiwan·Risk Class 2·K.F. MEDICAL INSTRUMENTS CO., LTD.·Registered Apr 06, 2006 – Apr 06, 2026Expired

Registration details

Analysis ID: 9adbf22257ae685cb60ca0cfc9cda91d
Customs Code: DHY00500174409

Company information

Manufacturer: K.F. MEDICAL INSTRUMENTS CO., LTD.
Manufacturer Country: Taiwan, Province of China
Authorized Representative: K.F. MEDICAL INSTRUMENTS CO., LTD.

Product details

Intended Use: For details, it is Chinese approved copy of the imitation order
Product Type (Level 1): I General, Plastic Surgery and Dermatology
Import Information: Domestic

Dates and status

Registration Date: Apr 06, 2006
Expiry Date: Apr 06, 2026

About this record

Access comprehensive regulatory information for "Guofa" iodine gauze strip in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 9adbf22257ae685cb60ca0cfc9cda91d and manufactured by K.F. MEDICAL INSTRUMENTS CO., LTD.. The authorized representative in Taiwan is K.F. MEDICAL INSTRUMENTS CO., LTD..

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