Taiwan FDA registration 6c0efb326bc437d973d7103d27a5d550

“DAEJU” ULTRA PULSE CO2 FRACTIONAL LASER

TW: “大州”二氧化碳雷射治療儀
Taiwan flagTaiwan·Risk Class 2·MD·DAEJU MEDITECH ENGINEERING Co., Ltd.·Registered Jan 12, 2023 – Jan 12, 2028Active
Registration details
Analysis ID
6c0efb326bc437d973d7103d27a5d550
License Form
Ministry of Health Medical Device Import No. 036280
Customs Code
DHA05603628007
Company information
Manufacturer Country
Korea, Republic of
Authorized Representative
Always Medical Co., Ltd
Product details
Intended Use
Details are as detailed as approved Chinese instructions
Product Type (Level 1)
I General, Plastic Surgery and Dermatology
Product Type (Level 2)
I4810 Lasers for general surgery, plastic surgery and dermatology
Import Information
Imported from abroad
Dates and status
Registration Date
Jan 12, 2023
Expiry Date
Jan 12, 2028
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About this record

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.

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