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“Remed” UI Cube Electromagnetic Stimulator - Taiwan Registration 4178507b8f83e6c8626b866b06166033

Access comprehensive regulatory information for “Remed” UI Cube 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 4178507b8f83e6c8626b866b06166033 and manufactured by REMED Co., Ltd.. The authorized representative in Taiwan is DERMACARE BIOMED 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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4178507b8f83e6c8626b866b06166033
Registration Details
Taiwan FDA Registration: 4178507b8f83e6c8626b866b06166033
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Device Details

“Remed” UI Cube Electromagnetic Stimulator
TW: “樂美” 優酷磁波刺激器
Risk Class 2
MD

Registration Details

4178507b8f83e6c8626b866b06166033

Ministry of Health Medical Device Import No. 036520

DHA05603652001

Company Information

Korea, Republic of

Product Details

Details are as detailed as approved Chinese instructions

H Gastroenterology and urology

H5320 Non-implantable electronic urination homemade device

Imported from abroad

Dates and Status

May 24, 2023

May 24, 2028