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“GENEMAX” Mechanical walker(Non-Sterile) - Taiwan Registration 34721241f42b1618dc687a096f55eb75

Access comprehensive regulatory information for “GENEMAX” Mechanical walker(Non-Sterile) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number 34721241f42b1618dc687a096f55eb75 and manufactured by GENEMAX MEDICAL PRODUCTS INDUSTRY CORP.. The authorized representative in Taiwan is GENEMAX MEDICAL PRODUCTS INDUSTRY CORP..

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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34721241f42b1618dc687a096f55eb75
Registration Details
Taiwan FDA Registration: 34721241f42b1618dc687a096f55eb75
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Device Details

“GENEMAX” Mechanical walker(Non-Sterile)
TW: “吉律”機械式助行器(未滅菌)
Risk Class 1
MD

Registration Details

34721241f42b1618dc687a096f55eb75

Ministry of Health Medical Device Manufacturing No. 008997

Company Information

Taiwan, Province of China

Product Details

Limited to the scope of Grade 1 identification of "Mechanical Mobility Aids (O.3825)" under the Measures for the Administration of Medical Devices.

o Equipment for physical medicine

O3825 Mechanical Mobility Aid

Produced in Taiwan, China

Dates and Status

Apr 08, 2021

Apr 08, 2026