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“VEINOPLUS” NEUROMUSCULAR STIMULATOR - Taiwan Registration 94edf83d9a2f3c8ce94a95943d4547c2

Access comprehensive regulatory information for “VEINOPLUS” NEUROMUSCULAR STIMULATOR in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 94edf83d9a2f3c8ce94a95943d4547c2 and manufactured by AD REM TECHNOLOGY;;For use only by the Parts System Denda. The authorized representative in Taiwan is WONDERVILLE 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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94edf83d9a2f3c8ce94a95943d4547c2
Registration Details
Taiwan FDA Registration: 94edf83d9a2f3c8ce94a95943d4547c2
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Device Details

“VEINOPLUS” NEUROMUSCULAR STIMULATOR
TW: “舒足健” 動力式肌肉刺激儀
Risk Class 2
MD

Registration Details

94edf83d9a2f3c8ce94a95943d4547c2

Ministry of Health Medical Device Import No. 035033

DHA05603503301

Company Information

Product Details

Details are as detailed as approved Chinese instructions

o Physical Medical Sciences

O5850 powered muscle stimulator

Imported from abroad

Dates and Status

Nov 19, 2021

Nov 19, 2026