Taiwan FDA registration 68687ead60f4dda28981be690fceb6a2

"K.F." CURING SHEET

TW: "國發"治療巾

Taiwan·Risk Class 2·MD·K.F. MEDICAL INSTRUMENTS CO., LTD.·Registered Apr 03, 2006 – Apr 03, 2026Expired

Registration details

Analysis ID: 68687ead60f4dda28981be690fceb6a2
License Form: Department of Health Medical Device Manufacturing No. 001737
Customs Code: DHY00500173702

Company information

Manufacturer: K.F. MEDICAL INSTRUMENTS CO., LTD.
Manufacturer Country: Taiwan, Province of China
Authorized Representative: Guofa Medical Equipment Co., Ltd

Product details

Intended Use: For details, it is Chinese approved copy of the imitation order
Product Type (Level 1): I General and plastic surgical devices
Import Information: Produced in Taiwan, China

Dates and status

Registration Date: Apr 03, 2006
Expiry Date: Apr 03, 2026

About this record

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.

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