"Medtronic" pediatric cannula with arterial root
- Analysis ID
- 212ea7e83ab5b139470dc9915054b3ae
- Customs Code
- DHA00601952508
- Manufacturer
- Medtronic Perfusion Systems;; Medtronic Inc.
- Manufacturer Country
- United States
- Authorized Representative
- MEDTRONIC (TAIWAN) LTD.
- 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.4210 Vascular catheters, cannulas and tubes for cardiopulmonary vascular bypassing
- Import Information
- import
- Registration Date
- Dec 24, 2008
- Expiry Date
- Dec 24, 2028
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Access comprehensive regulatory information for "Medtronic" pediatric cannula with arterial root in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 212ea7e83ab5b139470dc9915054b3ae 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, 1 companies making similar products including MEDTRONIC PERFUSION SYSTEMS, and 1 recent registrations in the same category. 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.