Taiwan FDA registration 54a357682928506ea37c14c451002ac9

“DAEJU” ULTRA PULSE CO2 FRACTIONAL LASER

TW: “太宇”二氧化碳雷射治療儀
Taiwan flagTaiwan·Risk Class 2·MD·DAEJU MEDITECH ENGINEERING·Registered Aug 08, 2018 – Aug 08, 2023Expired
Registration details
Analysis ID
54a357682928506ea37c14c451002ac9
License Form
Ministry of Health Medical Device Import No. 031389
Customs Code
DHA05603138904
Company information
Manufacturer Country
Korea, Republic of
Authorized Representative
YUNGLIN BIOTECHNOLOGY CO., LTD.
Product details
Intended Use
For details, it is Chinese approved copy of the imitation order
Product Type (Level 1)
I General and plastic surgical devices
Product Type (Level 2)
I4810 Lasers for general surgery, plastic surgery and dermatology
Import Information
Imported from abroad
Dates and status
Registration Date
Aug 08, 2018
Expiry Date
Aug 08, 2023
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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 54a357682928506ea37c14c451002ac9 and manufactured by DAEJU MEDITECH ENGINEERING. The authorized representative in Taiwan is YUNGLIN BIOTECHNOLOGY CO., LTD..

This page provides complete technical specifications, regulatory compliance details, 1 companies making similar products including DAEJU MEDITECH ENGINEERING Co., Ltd., 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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