"Medtronic" cardiac electrocautery system
Taiwan·Risk Class 2·Medtronic Perfusion Systems;; Medtronic Inc.·Registered Mar 21, 2022 – Mar 21, 2027Active- Analysis ID
- 50939d58e8f32eb35be9c2abaf7165f7
- Customs Code
- DHA05603535201
- Manufacturer
- Medtronic Perfusion Systems;; Medtronic Inc.
- Manufacturer Country
- United States
- Authorized Representative
- MEDTRONIC (TAIWAN) LTD.
- Intended Use
- Details are as detailed as approved Chinese instructions
- Product Type (Level 1)
- I General, Plastic Surgery and Dermatology
- Product Type (Level 2)
- I.4400 Cutting and hemostasis electric knives and accessories thereof
- Import Information
- import
- Registration Date
- Mar 21, 2022
- Expiry Date
- Mar 21, 2027
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Access comprehensive regulatory information for "Medtronic" cardiac electrocautery system in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 50939d58e8f32eb35be9c2abaf7165f7 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, 2 companies making similar products including Medtronic Perfusion Systems;; Medtronic Inc., Bovie Medical Corporation, and 2 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.