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Reiko limb equipment (unsterilized) - Taiwan Registration 42af75ff06619aad5cd8edcc595af8d2

Access comprehensive regulatory information for Reiko limb equipment (unsterilized) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number 42af75ff06619aad5cd8edcc595af8d2 and manufactured by Aimin Eisai Co., Ltd. Plant 2. The authorized representative in Taiwan is Aimin Eisai Co., Ltd. Plant 2.

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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42af75ff06619aad5cd8edcc595af8d2
Registration Details
Taiwan FDA Registration: 42af75ff06619aad5cd8edcc595af8d2
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Device Details

Reiko limb equipment (unsterilized)
TW: ้บ—ๅญ่‚ข้ซ”่ฃๅ…ท(ๆœชๆป…่Œ)
Risk Class 1
Cancelled

Registration Details

42af75ff06619aad5cd8edcc595af8d2

DHY04300129602

Company Information

Taiwan, Province of China

Product Details

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

o Physical Medical Sciences

O.3475 Limb fittings

Domestic

Dates and Status

Apr 20, 2006

Apr 20, 2016

May 10, 2018

Cancellation Information

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