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“KOIBIG” Transcutaneous Electrical Modulation System - Taiwan Registration a922317c0b696a1554fb41c33efe095d

Access comprehensive regulatory information for “KOIBIG” Transcutaneous Electrical Modulation System in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number a922317c0b696a1554fb41c33efe095d and manufactured by Mediver Inc.. The authorized representative in Taiwan is SERVICETECH INTERNATIONAL INC..

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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a922317c0b696a1554fb41c33efe095d
Registration Details
Taiwan FDA Registration: a922317c0b696a1554fb41c33efe095d
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Device Details

“KOIBIG” Transcutaneous Electrical Modulation System
TW: “科比”經皮神經電刺激器
Risk Class 2
MD

Registration Details

a922317c0b696a1554fb41c33efe095d

Ministry of Health Medical Device Import No. 034978

DHA05603497802

Company Information

Korea, Republic of

Product Details

Details are as detailed as approved Chinese instructions

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Dates and Status

Oct 21, 2021

Oct 21, 2026