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"Dayang" cold compress (unsterilized) - Taiwan Registration 4c9185242868e8a1b45453fdc7a8b97c

Access comprehensive regulatory information for "Dayang" 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 4c9185242868e8a1b45453fdc7a8b97c and manufactured by DIA PHARMACEUTICAL CO., LTD.. The authorized representative in Taiwan is Shengpu International Limited.

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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4c9185242868e8a1b45453fdc7a8b97c
Registration Details
Taiwan FDA Registration: 4c9185242868e8a1b45453fdc7a8b97c
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Device Details

"Dayang" cold compress (unsterilized)
TW: โ€œๅคง้™ฝโ€ๅ†ทๆ•ท่ฒผ (ๆœชๆป…่Œ)
Risk Class 1
Cancelled

Registration Details

4c9185242868e8a1b45453fdc7a8b97c

DHA04400661508

Company Information

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

import

Dates and Status

Mar 27, 2008

Mar 27, 2013

Jun 17, 2015

Cancellation Information

Logged out

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