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“Zimmer” ZFieldDual Magnetotherapy Device - Taiwan Registration ffde407187f3e5f9221be9d7082479dd

Access comprehensive regulatory information for “Zimmer” ZFieldDual 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 ffde407187f3e5f9221be9d7082479dd 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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ffde407187f3e5f9221be9d7082479dd
Registration Details
Taiwan FDA Registration: ffde407187f3e5f9221be9d7082479dd
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Device Details

“Zimmer” ZFieldDual Magnetotherapy Device
TW: “利麥爾” 立富多磁波治療器
Risk Class 2
MD

Registration Details

ffde407187f3e5f9221be9d7082479dd

Ministry of Health Medical Device Import No. 034528

DHA05603452807

Company Information

Germany

Product Details

Details are as detailed as approved Chinese instructions

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Imported from abroad

Dates and Status

May 14, 2021

May 14, 2026