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"Medtronic" cardiac electrocautery system - Taiwan Registration b2d541bdc75a1df2e55cdebcc8425a42

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.

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b2d541bdc75a1df2e55cdebcc8425a42
Registration Details
Taiwan FDA Registration: b2d541bdc75a1df2e55cdebcc8425a42
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Device Details

"Medtronic" cardiac electrocautery system
TW: โ€œ็พŽๆ•ฆๅŠ›โ€ๅฟƒ่‡Ÿ้›ป็‡’็ณป็ตฑ
Risk Class 2
Cancelled

Registration Details

b2d541bdc75a1df2e55cdebcc8425a42

DHA00601833307

Company Information

United States

Product Details

For details, it is Chinese approved copy of the imitation order.

I General, Plastic Surgery and Dermatology

I.4400 Cutting and hemostasis electric knives and accessories thereof

import

Dates and Status

Sep 21, 2007

Sep 21, 2017

Dec 15, 2015

Cancellation Information

Logged out

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