Taiwan FDA registration 7abb3bbb0b2040c2a9fa5c855e1fd4e8
“SINO” NC Thonic Non Compliant PTCA Balloon Dilatation Catheter
TW: “賽諾”速氝氪非順應性冠狀動脈氣球導管
Taiwan·Risk Class 2·MD·SINO Medical Sciences Technology Inc.·Registered Aug 31, 2018 – Aug 31, 2028ActiveRegistration details
- Analysis ID
- 7abb3bbb0b2040c2a9fa5c855e1fd4e8
- License Form
- Ministry of Health Medical Device Land Transport No. 000922
- Customs Code
- DHA09200092203
Company information
- Manufacturer
- SINO Medical Sciences Technology Inc.
- Manufacturer Country
- China
- Authorized Representative
- HAO YO ENTERPRISE CO., LTD.
Product details
- Intended Use
- For details, it is Chinese approved copy of the imitation order
- Product Type (Level 1)
- E Cardiovascular devices
- Product Type (Level 2)
- E0005 Percutaneous puncture of the coronary ductus
- Import Information
- Imported from abroad; Export;; Made in China
Dates and status
- Registration Date
- Aug 31, 2018
- Expiry Date
- Aug 31, 2028
About this record
Access comprehensive regulatory information for “SINO” NC Thonic Non Compliant PTCA Balloon Dilatation Catheter in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 7abb3bbb0b2040c2a9fa5c855e1fd4e8 and manufactured by SINO Medical Sciences Technology Inc.. The authorized representative in Taiwan is HAO YO ENTERPRISE CO., LTD..
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