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"GENTRY WAY" Crutch (Non-Sterile) - Taiwan Registration 3f4ed02a2276f716796bcdcaad8989e6

Access comprehensive regulatory information for "GENTRY WAY" Crutch (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 3f4ed02a2276f716796bcdcaad8989e6 and manufactured by GENTRY WAY CO., LTD.. The authorized representative in Taiwan is GENTRY WAY 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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3f4ed02a2276f716796bcdcaad8989e6
Registration Details
Taiwan FDA Registration: 3f4ed02a2276f716796bcdcaad8989e6
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Device Details

"GENTRY WAY" Crutch (Non-Sterile)
TW: "ไปฒ็พค็ถญ"้†ซ็™‚็”จๆ‹ๆ–(ๆœชๆป…่Œ)
Risk Class 1
MD

Registration Details

3f4ed02a2276f716796bcdcaad8989e6

Ministry of Health Medical Device Manufacturing Registration No. 004530

Company Information

Taiwan, Province of China

Product Details

Limited to the first level identification range of the Measures for the Administration of Medical Devices "Medical Canes (O.3150)".

o Equipment for physical medicine

O3150 Medical cane

Produced in Taiwan, China

Dates and Status

Oct 01, 2021

Oct 31, 2023