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“Zimmer”emFieldPro Magnetotherapy Device - Taiwan Registration 6cc0a0a327376dbbf0b4d430b3d6dc51

Access comprehensive regulatory information for “Zimmer”emFieldPro Magnetotherapy Device in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 6cc0a0a327376dbbf0b4d430b3d6dc51 and manufactured by ZIMMER MEDIZINSYSTEME GMBH. The authorized representative in Taiwan is WOH MEDICAL 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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6cc0a0a327376dbbf0b4d430b3d6dc51
Registration Details
Taiwan FDA Registration: 6cc0a0a327376dbbf0b4d430b3d6dc51
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Device Details

“Zimmer”emFieldPro Magnetotherapy Device
TW: “利麥爾”磁波治療器
Risk Class 2
MD

Registration Details

6cc0a0a327376dbbf0b4d430b3d6dc51

Ministry of Health Medical Device Import No. 035965

DHA05603596508

Company Information

Germany

Product Details

Details are as detailed as approved Chinese instructions

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Dates and Status

Oct 08, 2022

Oct 08, 2027