Taiwan FDA registration daaebb65f9ccba00eec25869044e7033
"Hangzhou Tianren" single-use linear cutting stapler and components
TW: “杭州天任”一次性使用直線型切割吻合器及組件
Taiwan·Risk Class 2·Hangzhou Tianren Bio-technology Co., Ltd·Registered Jan 13, 2017 – Jan 13, 2022CancelledRegistration details
- Analysis ID
- daaebb65f9ccba00eec25869044e7033
- Customs Code
- DHA09200079601
Company information
- Manufacturer
- Hangzhou Tianren Bio-technology Co., Ltd
- Manufacturer Country
- China
- Authorized Representative
- WELLONG 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
- Product Type (Level 2)
- I.4750 Implantable Joints
- Import Information
- Chinese goods;; input
Dates and status
- Registration Date
- Jan 13, 2017
- Expiry Date
- Jan 13, 2022
- Cancellation Date
- Apr 12, 2024
Cancellation information
- Status
- Logged out
- Reason
- 許可證已逾有效期
About this record
Access comprehensive regulatory information for "Hangzhou Tianren" single-use linear 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 daaebb65f9ccba00eec25869044e7033 and manufactured by Hangzhou Tianren Bio-technology Co., Ltd. The authorized representative in Taiwan is WELLONG INSTRUMENTS 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