"Medtronic" cardiac electrocautery system
- Analysis ID
- b2d541bdc75a1df2e55cdebcc8425a42
- Customs Code
- DHA00601833307
- Manufacturer
- Bovie Medical Corporation
- 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)
- 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
- Sep 21, 2007
- Expiry Date
- Sep 21, 2017
- Cancellation Date
- Dec 15, 2015
- Status
- Logged out
- Reason
- 自請註銷
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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 b2d541bdc75a1df2e55cdebcc8425a42 and manufactured by Bovie Medical Corporation. 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;; Medtronic Inc., 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.