Taiwan FDA registration 5a9657d82d5b83d3c3a9b318163b5c89
"INSZO" aortic balloon catheter
TW: “英斯卓”主動脈氣球導管
Taiwan·Risk Class 2·Insightra Medical, Inc.·Registered Mar 28, 2017 – Mar 28, 2022CancelledRegistration details
- Analysis ID
- 5a9657d82d5b83d3c3a9b318163b5c89
- Customs Code
- DHA05602942809
Company information
- Manufacturer
- Insightra Medical, Inc.
- Manufacturer Country
- United States
- Authorized Representative
- HSIN TUNG MEDICAL CO., LTD.
Product details
- Intended Use
- For details, it is Chinese approved copy of the imitation order
- Product Type (Level 1)
- E Cardiovascular Medicine Science
- Product Type (Level 2)
- E.3535 Intraarchary Aortic Balloon Dilation and Control System
- Import Information
- Contract manufacturing;; input
Dates and status
- Registration Date
- Mar 28, 2017
- Expiry Date
- Mar 28, 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 "INSZO" aortic balloon catheter in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 5a9657d82d5b83d3c3a9b318163b5c89 and manufactured by Insightra Medical, Inc.. The authorized representative in Taiwan is HSIN TUNG MEDICAL 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