Taiwan FDA registration b2d541bdc75a1df2e55cdebcc8425a42

"Medtronic" cardiac electrocautery system

TW: “美敦力”心臟電燒系統
Taiwan flagTaiwan·Risk Class 2·Bovie Medical Corporation·Registered Sep 21, 2007 – Sep 21, 2017Cancelled
Registration details
Analysis ID
b2d541bdc75a1df2e55cdebcc8425a42
Customs Code
DHA00601833307
Company information
Manufacturer Country
United States
Authorized Representative
MEDTRONIC (TAIWAN) LTD.
Product details
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
Dates and status
Registration Date
Sep 21, 2007
Expiry Date
Sep 21, 2017
Cancellation Date
Dec 15, 2015
Cancellation information
Status
Logged out
Reason
自請註銷
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About this record

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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