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“J.P.”Cushion (Non-Sterile) - Taiwan Registration f5884425cc3d24ca5277dfce7c5d09df

Access comprehensive regulatory information for “J.P.”Cushion (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 f5884425cc3d24ca5277dfce7c5d09df and manufactured by SEALTECH., LTD. The authorized representative in Taiwan is J. P. 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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f5884425cc3d24ca5277dfce7c5d09df
Registration Details
Taiwan FDA Registration: f5884425cc3d24ca5277dfce7c5d09df
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Device Details

“J.P.”Cushion (Non-Sterile)
TW: “建鵬”浮動坐墊 (未滅菌)
Risk Class 1
MD

Registration Details

f5884425cc3d24ca5277dfce7c5d09df

Ministry of Health Medical Device Import No. 017703

DHA09401770309

Company Information

Korea, Republic of

Product Details

Limited to the first level identification scope of the Measures for the Administration of Medical Equipment "Floating Cushion (O.3175)".

o Equipment for physical medicine

O3175 floating seat cushion

Imported from abroad

Dates and Status

Apr 12, 2017

Apr 12, 2022