Taiwan FDA registration 97f65809c7f4938be939a423cb91e3ff
Guofa puncture dressing preparation kit
TW: 國發穿刺敷料準備包
Taiwan·Risk Class 2·Guofa Medical Equipment Co., Ltd. factory·Registered Jun 01, 2006 – Jun 01, 2026ExpiredRegistration details
- Analysis ID
- 97f65809c7f4938be939a423cb91e3ff
- Customs Code
- DHY00500182407
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
- 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
- Jun 01, 2006
- Expiry Date
- Jun 01, 2026
About this record
Access comprehensive regulatory information for Guofa puncture dressing preparation kit in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 97f65809c7f4938be939a423cb91e3ff 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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