Pure Global

"Medis" diode laser treatment instrument and its accessories - Taiwan Registration 420e2e23c9dc0b7e2d182653dfa9b74f

Access comprehensive regulatory information for "Medis" diode laser treatment instrument and its accessories in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 420e2e23c9dc0b7e2d182653dfa9b74f and manufactured by SURGICAL LASER TECHNOLOGIES, A DIVISION OF PHOTOMEDEX, INC.. The authorized representative in Taiwan is LITE-MED INC..

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
420e2e23c9dc0b7e2d182653dfa9b74f
Registration Details
Taiwan FDA Registration: 420e2e23c9dc0b7e2d182653dfa9b74f
Pure Global
DJ Fang

DJ Fang

MedTech Regulatory Expert

Need help with 30+ markets registration?

Pricing

Device Details

"Medis" diode laser treatment instrument and its accessories
TW: โ€œ้บฅ่ฟชๆ–ฏโ€ไบŒๆฅต้ซ”้›ทๅฐ„ๆฒป็™‚ๅ„€ๅŠๅ…ถ้…ไปถ
Risk Class 2
Cancelled

Registration Details

420e2e23c9dc0b7e2d182653dfa9b74f

DHA00601934901

Company Information

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

import

Dates and Status

Nov 14, 2008

Nov 14, 2013

May 28, 2015

Cancellation Information

Logged out

่จฑๅฏ่ญ‰ๅทฒ้€พๆœ‰ๆ•ˆๆœŸ