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“REMED” Electromagnetic Stimulator - Taiwan Registration 25905a06a9da5bfa59d57217ec1121ca

Access comprehensive regulatory information for “REMED” Electromagnetic Stimulator in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 25905a06a9da5bfa59d57217ec1121ca and manufactured by Remed Co., Ltd.. The authorized representative in Taiwan is BP BIOTECHNOLOGY COMPANY.

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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25905a06a9da5bfa59d57217ec1121ca
Registration Details
Taiwan FDA Registration: 25905a06a9da5bfa59d57217ec1121ca
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Device Details

“REMED” Electromagnetic Stimulator
TW: “樂密”磁波刺激器
Risk Class 2
MD

Registration Details

25905a06a9da5bfa59d57217ec1121ca

Ministry of Health Medical Device Import No. 034817

DHA05603481701

Company Information

Korea, Republic of

Product Details

Details are as detailed as approved Chinese instructions

Ø Devices for physical medicine;; K Apparatus for neurology

O5850 Powered Muscle Stimulator;; K5890 Transcutaneous electrical nerve stimulator for pain relief

Imported from abroad

Dates and Status

Aug 13, 2021

Aug 13, 2026