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“Lumenis” ResurFx Laser System - Taiwan Registration 9b360cfaba2c811881fc430d620e2956

Access comprehensive regulatory information for “Lumenis” ResurFx Laser System in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 9b360cfaba2c811881fc430d620e2956 and manufactured by LUMENIS LTD.. The authorized representative in Taiwan is (Hong Kong) Lumenis Be (HK) Limited, Taiwan Branch.

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.

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9b360cfaba2c811881fc430d620e2956
Registration Details
Taiwan FDA Registration: 9b360cfaba2c811881fc430d620e2956
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Device Details

“Lumenis” ResurFx Laser System
TW: “洛明尼斯”梭時雷射系統
Risk Class 2
MD

Registration Details

9b360cfaba2c811881fc430d620e2956

Ministry of Health Medical Device Import No. 028634

DHA05602863407

Company Information

Israel

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

Jul 19, 2016

Jul 19, 2026