Taiwan FDA registration fe56105f9d989ec0b526b7247c01b04e

"Kangis Mei" antipyretic patch (unsterilized)

TW: “康是美” 退熱貼片 (未滅菌)

Taiwan·Risk Class 1·Desheng Pharmaceutical Co., Ltd. Plant 2·Registered Nov 07, 2012 – Nov 07, 2017Cancelled

Registration details

Analysis ID: fe56105f9d989ec0b526b7247c01b04e

Company information

Manufacturer: Desheng Pharmaceutical Co., Ltd. Plant 2
Manufacturer Country: Taiwan, Province of China
Authorized Representative: PRESIDENT DRUGSTORE BUSINESS CORPORATION

Product details

Intended Use: Limited to the first level identification range of the Measures for the Administration of Medical Equipment "Medical Cold Compress Pack (O.5700)".
Product Type (Level 1): o Physical Medical Sciences
Product Type (Level 2): O.5700 醫療用冷熱敷裝置
Import Information: Domestic;; Contract manufacturing

Dates and status

Registration Date: Nov 07, 2012
Expiry Date: Nov 07, 2017
Cancellation Date: Dec 13, 2019

Cancellation information

Status: Logged out
Reason: 許可證已逾有效期

About this record

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.