Pure Global

"Kanghe" multi-channel laser irradiation instrument - Taiwan Registration efbdfe6fe03550a0e5fbfd8fec901b0e

Access comprehensive regulatory information for "Kanghe" multi-channel laser irradiation instrument in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number efbdfe6fe03550a0e5fbfd8fec901b0e and manufactured by KONFTEC CORPORATION. The authorized representative in Taiwan is KONFTEC CORPORATION.

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
efbdfe6fe03550a0e5fbfd8fec901b0e
Registration Details
Taiwan FDA Registration: efbdfe6fe03550a0e5fbfd8fec901b0e
Pure Global
DJ Fang

DJ Fang

MedTech Regulatory Expert

Need help with 30+ markets registration?

Pricing

Device Details

"Kanghe" multi-channel laser irradiation instrument
TW: โ€œๅบท็ฆพโ€ๅคš้ ป้“้›ทๅฐ„็…งๅฐ„ๅ„€
Risk Class 2

Registration Details

efbdfe6fe03550a0e5fbfd8fec901b0e

DHY00500256300

Company Information

Taiwan, Province of China

Product Details

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

I General, Plastic Surgery and Dermatology

I.4810 Lasers for general surgical, orthopaedic and dermatological use

Domestic

Dates and Status

Dec 05, 2008

Dec 05, 2028