Taiwan FDA registration e8064ceb2762675ba2afa2165bfb7dd2

"Platinum" antipyretic patch (unsterilized)

TW: “白金”退熱貼(未滅菌)
Taiwan flagTaiwan·Risk Class 1·DIA PHARMACEUTICAL CO., LTD.·Registered Oct 24, 2007 – Oct 24, 2022Cancelled
Registration details
Analysis ID
e8064ceb2762675ba2afa2165bfb7dd2
Customs Code
DHA04400624603
Company information
Manufacturer Country
Japan
Authorized Representative
SMILER CO., LTD.
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
import
Dates and status
Registration Date
Oct 24, 2007
Expiry Date
Oct 24, 2022
Cancellation Date
Sep 30, 2021
Cancellation information
Status
Logged out
Reason
轉為登錄字號
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About this record

Access comprehensive regulatory information for "Platinum" 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 e8064ceb2762675ba2afa2165bfb7dd2 and manufactured by DIA PHARMACEUTICAL CO., LTD.. The authorized representative in Taiwan is SMILER CO., LTD..

This page provides complete technical specifications, regulatory compliance details, 1 companies making similar products including DIA PHARMACEUTICAL CO., LTD., and 1 recent registrations in the same category. 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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