Taiwan FDA registration e76764b5b7dbbdb0e74cd490fccd6310
"Qiwei" compression arterial hemostat (unsterilized)
TW: "奇維" 壓迫式動脈止血器 (未滅菌)
Taiwan·Risk Class 1·KEWEI RISING MEDICAL GROUP LTD.·Registered Jul 07, 2016 – Jul 07, 2021CancelledRegistration details
- Analysis ID
- e76764b5b7dbbdb0e74cd490fccd6310
- Customs Code
- DHA09600277506
Company information
- Manufacturer
- KEWEI RISING MEDICAL GROUP LTD.
- Manufacturer Country
- China
- Authorized Representative
- CATHERINE CONSULTANTS CO., LTD.
Product details
- Intended Use
- Limited to the first level identification range of the Measures for the Administration of Medical Devices "Non-inflatable Tourniquet (I.5900)".
- Product Type (Level 1)
- I General, Plastic Surgery and Dermatology
- Product Type (Level 2)
- I.5900 非充氣式止血帶
- Import Information
- Chinese goods;; input
Dates and status
- Registration Date
- Jul 07, 2016
- Expiry Date
- Jul 07, 2021
- Cancellation Date
- Oct 06, 2023
Cancellation information
- Status
- Logged out
- Reason
- 自行鍵入
About this record
Access comprehensive regulatory information for "Qiwei" compression arterial hemostat (unsterilized) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number e76764b5b7dbbdb0e74cd490fccd6310 and manufactured by KEWEI RISING MEDICAL GROUP LTD.. The authorized representative in Taiwan is CATHERINE 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