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"CAPRON" Corrective Insole (Non-Sterile) - Taiwan Registration d014034fe801e3f5c8b3c28a51f929df

Access comprehensive regulatory information for "CAPRON" 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 d014034fe801e3f5c8b3c28a51f929df and manufactured by CAPRON PODOLOGIE. The authorized representative in Taiwan is UHEALTH COMPANY LIMITED.

This page provides complete technical specifications, regulatory compliance details, 1 companies making similar products including CAPRON PODOLOGIE, and 1 recent registrations in the same category. 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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d014034fe801e3f5c8b3c28a51f929df
Registration Details
Taiwan FDA Registration: d014034fe801e3f5c8b3c28a51f929df
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Device Details

"CAPRON" Corrective Insole (Non-Sterile)
TW: "ๅ‡ฑๆ™ฎๅ€ซ" ็Ÿฏๆญฃ้ž‹ๅขŠ(ๆœชๆป…่Œ)
Risk Class 1
MD

Registration Details

d014034fe801e3f5c8b3c28a51f929df

Ministry of Health Medical Device Import Registration No. 019701

DHA08401970106

Company Information

France

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, 2023

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