Pure Global

“Lumenis” OtoLase System - Taiwan Registration a871fb257441899af700cb26e99c3ddd

Access comprehensive regulatory information for “Lumenis” OtoLase System in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number a871fb257441899af700cb26e99c3ddd and manufactured by LUMENIS LTD.. The authorized representative in Taiwan is BOSTON SCIENTIFIC INTERNATIONAL B.V., TAIWAN BRANCH (NETHERLANDS).

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.

Free Database
Powered by Pure Global AI
89,000+ Devices
a871fb257441899af700cb26e99c3ddd
Registration Details
Taiwan FDA Registration: a871fb257441899af700cb26e99c3ddd
Pure Global
DJ Fang

DJ Fang

MedTech Regulatory Expert

Need help with 30+ markets registration?

Pricing

Device Details

“Lumenis” OtoLase System
TW: “洛明尼斯”歐特雷系統
Risk Class 2
MD

Registration Details

a871fb257441899af700cb26e99c3ddd

Ministry of Health Medical Device Import No. 030947

DHA05603094707

Company Information

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

Mar 05, 2018

Mar 05, 2028