Taiwan FDA registration d940fd5c234ae9f08373443481fd87b9
"K.F."SURGICAL APPAREL PACK
TW: "國發"手術衣物包
Taiwan·Risk Class 2·MD·Guofa Medical Equipment Co., Ltd·Registered May 30, 2006 – May 30, 2026ExpiredRegistration details
- Analysis ID
- d940fd5c234ae9f08373443481fd87b9
- License Form
- Department of Health Medical Device Manufacturing No. 001823
- Customs Code
- DHY00500182305
Company information
- Manufacturer
- Guofa Medical Equipment 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
- May 30, 2006
- Expiry Date
- May 30, 2026
About this record
Access comprehensive regulatory information for "K.F."SURGICAL APPAREL PACK in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number d940fd5c234ae9f08373443481fd87b9 and manufactured by Guofa Medical Equipment Co., Ltd. The authorized representative in Taiwan is Guofa Medical Equipment Co., Ltd.
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