Pure Global

"Powerway" eye cauter - Taiwan Registration 95a2570685f4603caa66930dd463d244

Access comprehensive regulatory information for "Powerway" eye cauter in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 95a2570685f4603caa66930dd463d244 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.

Free Database
Powered by Pure Global AI
89,000+ Devices
95a2570685f4603caa66930dd463d244
Registration Details
Taiwan FDA Registration: 95a2570685f4603caa66930dd463d244
Pure Global
DJ Fang

DJ Fang

MedTech Regulatory Expert

Need help with 30+ markets registration?

Pricing

Device Details

"Powerway" eye cauter
TW: "ไฟๅจ" ็œผ็”จ็‡’็ผๅ™จ
Risk Class 2

Registration Details

95a2570685f4603caa66930dd463d244

DHA00601373301

Company Information

United States

Product Details

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

M Ophthalmology

M.4115 Thermal cauterizer

import

Dates and Status

Dec 05, 2005

Dec 05, 2025