Taiwan FDA registration 93d8257ec80cd8a3443c159ede721948
"Yisi Suzhou" disposable laparoscope with straight cutting stapler and components
TW: “逸思蘇州”一次性腔鏡用直線型切割吻合器及組件
Taiwan·Risk Class 2·Ezisurg (Suzhou) Medical Co., Ltd.·Registered Mar 31, 2022 – Mar 31, 2027ActiveRegistration details
- Analysis ID
- 93d8257ec80cd8a3443c159ede721948
- Customs Code
- DHA09200131602
Company information
- Manufacturer
- Ezisurg (Suzhou) Medical Co., Ltd.
- Manufacturer Country
- China
- Authorized Representative
- DR SHAO MD REGULATORY CONSULTANTS 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
- Chinese goods;; input
Dates and status
- Registration Date
- Mar 31, 2022
- Expiry Date
- Mar 31, 2027
About this record
Access comprehensive regulatory information for "Yisi Suzhou" disposable laparoscope with straight cutting stapler and components in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 93d8257ec80cd8a3443c159ede721948 and manufactured by Ezisurg (Suzhou) Medical Co., Ltd.. The authorized representative in Taiwan is DR SHAO MD REGULATORY CONSULTANTS CO., LTD..
This page provides complete technical specifications, regulatory compliance details. Pure Global AI offers free access to 89,000+ Taiwan medical device registrations, helping global MedTech companies navigate Taiwan FDA regulations, identify competitors, and discover partnership opportunities efficiently.
Free DatabasePowered by Pure Global AI89,000+ Devices