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"Powerway" surgical electrocautery - Taiwan Registration 923f391d3784ec1d27756001b3874d9f

Access comprehensive regulatory information for "Powerway" surgical electrocautery in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 923f391d3784ec1d27756001b3874d9f and manufactured by Bovie Medical Corporation. The authorized representative in Taiwan is KINGJING INTERNATIONAL 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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923f391d3784ec1d27756001b3874d9f
Registration Details
Taiwan FDA Registration: 923f391d3784ec1d27756001b3874d9f
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Device Details

"Powerway" surgical electrocautery
TW: "ไฟๅจ" ๆ‰‹่ก“้›ป็‡’ๅˆ€
Risk Class 2

Registration Details

923f391d3784ec1d27756001b3874d9f

DHA00601190606

Company Information

United States

Product Details

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

I General, Plastic Surgery and Dermatology

import

Dates and Status

Sep 13, 2005

Sep 13, 2025