Taiwan FDA registration 41da6a3de781c68dcd550a8dec59e475
Ikemo membrane artificial heart-lung
TW: 艾克模薄膜式人工心肺
Registration details
- Analysis ID
- 41da6a3de781c68dcd550a8dec59e475
- Customs Code
- DHA00600946204
Company information
- Manufacturer
- MEDTRONIC PERFUSION SYSTEMS
- Manufacturer Country
- United States
- Authorized Representative
- MEDTRONIC (TAIWAN) LTD.
Product details
- Product Type (Level 1)
- 9999 Other
- Import Information
- import
Dates and status
- Registration Date
- Jul 26, 2000
- Expiry Date
- Jul 26, 2015
- Cancellation Date
- Apr 25, 2018
Cancellation information
- Status
- Logged out
- Reason
- 自行鍵入
About this record
Access comprehensive regulatory information for Ikemo membrane artificial heart-lung in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 3 medical device is registered under number 41da6a3de781c68dcd550a8dec59e475 and manufactured by MEDTRONIC PERFUSION SYSTEMS. 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