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"Desheng" cold compress (unsterilized) - Taiwan Registration 4ea92a73d3cdb5db4886f927deac06e8

Access comprehensive regulatory information for "Desheng" cold compress (unsterilized) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number 4ea92a73d3cdb5db4886f927deac06e8 and manufactured by Desheng Pharmaceutical Co., Ltd. Plant 2. The authorized representative in Taiwan is Desheng Pharmaceutical 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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4ea92a73d3cdb5db4886f927deac06e8
Registration Details
Taiwan FDA Registration: 4ea92a73d3cdb5db4886f927deac06e8
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Device Details

"Desheng" cold compress (unsterilized)
TW: โ€œๅพ—็”Ÿโ€ๅ†ทๆ•ท่ฒผ(ๆœชๆป…่Œ)
Risk Class 1
Cancelled

Registration Details

4ea92a73d3cdb5db4886f927deac06e8

Company Information

Taiwan, Province of China

Product Details

Limited to the first level identification range of the Measures for the Administration of Medical Equipment "Medical Cold Compress Pack (O.5700)".

o Physical Medical Sciences

O.5700 ้†ซ็™‚็”จๅ†ท็†ฑๆ•ท่ฃ็ฝฎ

Domestic

Dates and Status

Jun 16, 2011

Jun 16, 2026

Sep 30, 2021

Cancellation Information

Logged out

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