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Hi-Life Antipyretic Patch (Unsterilized) - Taiwan Registration dfd2ec8ebfdbe7d349a672b6f6acd10a

Access comprehensive regulatory information for Hi-Life 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 dfd2ec8ebfdbe7d349a672b6f6acd10a and manufactured by TAIWAN STANCH CO., LTD.. The authorized representative in Taiwan is HI-LIFE INTERNATIONAL CO., LTD..

This page provides complete technical specifications, regulatory compliance details, 1 companies making similar products including Laierfu International Company Limited;; Taiwan Shujie 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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dfd2ec8ebfdbe7d349a672b6f6acd10a
Registration Details
Taiwan FDA Registration: dfd2ec8ebfdbe7d349a672b6f6acd10a
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Device Details

Hi-Life Antipyretic Patch (Unsterilized)
TW: Hi-Life ้€€็†ฑ่ฒผ็‰‡ (ๆœชๆป…่Œ)
Risk Class 1
Cancelled

Registration Details

dfd2ec8ebfdbe7d349a672b6f6acd10a

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

Mar 21, 2017

Mar 21, 2022

Sep 30, 2021

Cancellation Information

Logged out

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