Taiwan FDA registration dfd2ec8ebfdbe7d349a672b6f6acd10a

Hi-Life Antipyretic Patch (Unsterilized)

TW: Hi-Life 退熱貼片 (未滅菌)
Taiwan flagTaiwan·Risk Class 1·TAIWAN STANCH CO., LTD.·Registered Mar 21, 2017 – Mar 21, 2022Cancelled
Registration details
Analysis ID
dfd2ec8ebfdbe7d349a672b6f6acd10a
Company information
Manufacturer Country
Taiwan, Province of China
Authorized Representative
HI-LIFE INTERNATIONAL 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
Domestic;; Contract manufacturing
Dates and status
Registration Date
Mar 21, 2017
Expiry Date
Mar 21, 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 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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