Pure Global

“DAEJU” ULTRA PULSE CO2 FRACTIONAL LASER - Taiwan Registration 6c0efb326bc437d973d7103d27a5d550

Access comprehensive regulatory information for “DAEJU” ULTRA PULSE CO2 FRACTIONAL LASER in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 6c0efb326bc437d973d7103d27a5d550 and manufactured by DAEJU MEDITECH ENGINEERING Co., Ltd.. The authorized representative in Taiwan is Always Medical Co., Ltd.

This page provides complete technical specifications, regulatory compliance details, 1 companies making similar products including DAEJU MEDITECH ENGINEERING, and 1 recent registrations in the same category. 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
1 Competitors
1 Recent Registrations
6c0efb326bc437d973d7103d27a5d550
Registration Details
Taiwan FDA Registration: 6c0efb326bc437d973d7103d27a5d550
Pure Global
DJ Fang

DJ Fang

MedTech Regulatory Expert

Need help with 30+ markets registration?

Pricing

Device Details

“DAEJU” ULTRA PULSE CO2 FRACTIONAL LASER
TW: “大州”二氧化碳雷射治療儀
Risk Class 2
MD

Registration Details

6c0efb326bc437d973d7103d27a5d550

Ministry of Health Medical Device Import No. 036280

DHA05603628007

Company Information

Korea, Republic of

Product Details

Details are as detailed as approved Chinese instructions

I General, Plastic Surgery and Dermatology

I4810 Lasers for general surgery, plastic surgery and dermatology

Imported from abroad

Dates and Status

Jan 12, 2023

Jan 12, 2028

Companies Making Similar Products
Top companies providing products similar to "“DAEJU” ULTRA PULSE CO2 FRACTIONAL LASER"