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“DAEJU” ULTRA PULSE CO2 FRACTIONAL LASER - Taiwan Registration 54a357682928506ea37c14c451002ac9

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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54a357682928506ea37c14c451002ac9
Registration Details
Taiwan FDA Registration: 54a357682928506ea37c14c451002ac9
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Device Details

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

Registration Details

54a357682928506ea37c14c451002ac9

Ministry of Health Medical Device Import No. 031389

DHA05603138904

Company Information

Korea, Republic of

Product Details

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

I General and plastic surgical devices

I4810 Lasers for general surgery, plastic surgery and dermatology

Imported from abroad

Dates and Status

Aug 08, 2018

Aug 08, 2023

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