Taiwan FDA registration 8cd690e8a9135388b89f9c02c30a42d7
"Rip" single-use laparoscopic cutting stapler and laparoscopic assembly
TW: “瑞普”一次性使用腔鏡切割吻合器及腔鏡組件
Taiwan·Risk Class 2·Jiangsu Ripe Medical Instruments Technology Co., Ltd.·Registered Jan 17, 2023 – Jan 17, 2028ActiveRegistration details
- Analysis ID
- 8cd690e8a9135388b89f9c02c30a42d7
- Customs Code
- DHA09200142800
Company information
- Manufacturer Country
- China
- Authorized Representative
- MED INTERNATIONAL MARKETING CO., LTD.
Product details
- Intended Use
- Details are as detailed as approved Chinese instructions
- Product Type (Level 1)
- I General, Plastic Surgery and Dermatology
- Product Type (Level 2)
- I.4750 Implantable Joints
- Import Information
- Input;; Chinese goods
Dates and status
- Registration Date
- Jan 17, 2023
- Expiry Date
- Jan 17, 2028
About this record
Access comprehensive regulatory information for "Rip" single-use laparoscopic cutting stapler and laparoscopic assembly in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 8cd690e8a9135388b89f9c02c30a42d7 and manufactured by Jiangsu Ripe Medical Instruments Technology Co., Ltd.. The authorized representative in Taiwan is MED INTERNATIONAL MARKETING CO., LTD..
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