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“Lutronic”CoreLevee Electromagnetic Stimulator System - Taiwan Registration 4b8b1ac1cf7b21b79bf22a84933a4c5d

Access comprehensive regulatory information for “Lutronic”CoreLevee Electromagnetic Stimulator System in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 4b8b1ac1cf7b21b79bf22a84933a4c5d and manufactured by LUTRONIC CORPORATION. The authorized representative in Taiwan is K&C MEDICAL CO., LTD..

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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Registration Details
Taiwan FDA Registration: 4b8b1ac1cf7b21b79bf22a84933a4c5d
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Device Details

“Lutronic”CoreLevee Electromagnetic Stimulator System
TW: “璐霓可”磁波刺激系統
Risk Class 2
MD

Registration Details

4b8b1ac1cf7b21b79bf22a84933a4c5d

Ministry of Health Medical Device Import No. 035962

DHA05603596202

Company Information

Korea, Republic of

Product Details

Details are as detailed as approved Chinese instructions

o Physical Medical Sciences

O5850 powered muscle stimulator

Imported from abroad

Dates and Status

Oct 08, 2022

Oct 08, 2027