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“ENDOVISION” Radiofrequency Plasma Electrosurgical system - Taiwan Registration 9680f90b19c1f112efcbb70920932928

Access comprehensive regulatory information for “ENDOVISION” Radiofrequency Plasma Electrosurgical system in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 9680f90b19c1f112efcbb70920932928 and manufactured by ENDOVISION CO., LTD. The authorized representative in Taiwan is BAUI BIOTECH CO., LTD..

This page provides complete technical specifications, regulatory compliance details. 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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9680f90b19c1f112efcbb70920932928
Registration Details
Taiwan FDA Registration: 9680f90b19c1f112efcbb70920932928
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Device Details

“ENDOVISION” Radiofrequency Plasma Electrosurgical system
TW: “恩多威視”手術用電燒刀系統
Risk Class 2
MD

Registration Details

9680f90b19c1f112efcbb70920932928

Ministry of Health Medical Device Import No. 036655

DHA05603665501

Company Information

Korea, Republic of

Product Details

Details are as detailed as approved Chinese instructions

I General, Plastic Surgery and Dermatology

I4400 Electric knife for cutting and hemostasis and its accessories

Imported from abroad

Dates and Status

Jun 26, 2023

Jun 26, 2028