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“NOLARO”Medical Corrective Insole (Non-Sterile) - Taiwan Registration a423abe515b17ca4294aed60f99d3a38

Access comprehensive regulatory information for “NOLARO”Medical Corrective Insole (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 a423abe515b17ca4294aed60f99d3a38 and manufactured by NOLARO 24 LLC.. The authorized representative in Taiwan is Heavy Maintenance Rehabilitation Products 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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a423abe515b17ca4294aed60f99d3a38
Registration Details
Taiwan FDA Registration: a423abe515b17ca4294aed60f99d3a38
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Device Details

“NOLARO”Medical Corrective Insole (Non-Sterile)
TW: “諾拉柔”醫用矯正鞋墊(未滅菌)
Risk Class 1
MD

Registration Details

a423abe515b17ca4294aed60f99d3a38

Ministry of Health Medical Device Import Registration No. 009061

DHA08400906103

Company Information

United States

Product Details

Limited to the first level recognition range of limb equipment (O.3475) of the Measures for the Administration of Medical Devices.

o Equipment for physical medicine

O3475 Body Equipment

Imported from abroad

Dates and Status

Oct 01, 2021

Oct 31, 2025