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"Kangis Mei" antipyretic patch (unsterilized) - Taiwan Registration fe56105f9d989ec0b526b7247c01b04e

Access comprehensive regulatory information for "Kangis Mei" antipyretic patch (unsterilized) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number fe56105f9d989ec0b526b7247c01b04e and manufactured by Desheng Pharmaceutical Co., Ltd. Plant 2. The authorized representative in Taiwan is PRESIDENT DRUGSTORE BUSINESS CORPORATION.

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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fe56105f9d989ec0b526b7247c01b04e
Registration Details
Taiwan FDA Registration: fe56105f9d989ec0b526b7247c01b04e
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Device Details

"Kangis Mei" antipyretic patch (unsterilized)
TW: โ€œๅบทๆ˜ฏ็พŽโ€ ้€€็†ฑ่ฒผ็‰‡ (ๆœชๆป…่Œ)
Risk Class 1
Cancelled

Registration Details

fe56105f9d989ec0b526b7247c01b04e

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;; Contract manufacturing

Dates and Status

Nov 07, 2012

Nov 07, 2017

Dec 13, 2019

Cancellation Information

Logged out

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