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“VEINOPLUS”NEUROMUSCULAR STIMULATOR - Taiwan Registration 1b55501634199e664efd38e62e65d5a1

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 1b55501634199e664efd38e62e65d5a1 and manufactured by AD REM TECHNOLOGY. 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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1b55501634199e664efd38e62e65d5a1
Registration Details
Taiwan FDA Registration: 1b55501634199e664efd38e62e65d5a1
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Device Details

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

Registration Details

1b55501634199e664efd38e62e65d5a1

Ministry of Health Medical Device Import No. 035416

DHA05603541601

Company Information

France

Product Details

Details are as detailed as approved Chinese instructions

o Physical Medical Sciences

O5850 powered muscle stimulator

Imported from abroad

Dates and Status

Apr 26, 2022

Apr 26, 2027