Taiwan FDA registration c5b05fae2d2b65b10b2944e7f07dc9ad
"Yisi Suzhou" single-use tube stapler
TW: “逸思蘇州”一次性使用管型吻合器
Taiwan·Risk Class 2·Ezisurg (Suzhou) Medical Co., Ltd.·Registered Mar 01, 2020 – Mar 01, 2025ExpiredRegistration details
- Analysis ID
- c5b05fae2d2b65b10b2944e7f07dc9ad
- Customs Code
- DHA09200111607
Company information
- Manufacturer
- Ezisurg (Suzhou) Medical Co., Ltd.
- Manufacturer Country
- China
- Authorized Representative
- DR SHAO MD REGULATORY CONSULTANTS 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
- Product Type (Level 2)
- I.4750 Implantable Joints
- Import Information
- Input;; Chinese goods
Dates and status
- Registration Date
- Mar 01, 2020
- Expiry Date
- Mar 01, 2025
About this record
Access comprehensive regulatory information for "Yisi Suzhou" single-use tube stapler in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number c5b05fae2d2b65b10b2944e7f07dc9ad and manufactured by Ezisurg (Suzhou) Medical Co., Ltd.. The authorized representative in Taiwan is DR SHAO MD REGULATORY CONSULTANTS CO., LTD..
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