Taiwan FDA registration b8970a9a8529caa2484dbbd56e20a8cf
Coronary orifice perfusion cannula
TW: 冠狀動脈口灌流套管
Registration details
- Analysis ID
- b8970a9a8529caa2484dbbd56e20a8cf
- Customs Code
- DHA00600923901
Company information
- Manufacturer
- Medtronic Perfusion Systems;; Medtronic Inc.
- Manufacturer Country
- United States
- Authorized Representative
- MEDTRONIC (TAIWAN) LTD.
Product details
- Product Type (Level 1)
- 0699 Other Intensive Care Unit & Cardiac Care Unit Equipment
- Import Information
- import
Dates and status
- Registration Date
- Jul 06, 1999
- Expiry Date
- Feb 09, 2029
About this record
Access comprehensive regulatory information for Coronary orifice perfusion cannula in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number b8970a9a8529caa2484dbbd56e20a8cf and manufactured by Medtronic Perfusion Systems;; Medtronic Inc.. The authorized representative in Taiwan is MEDTRONIC (TAIWAN) 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