Taiwan FDA registration 4e6bea6c4dc3082cb8e89718b28b0cd8

Hi-Life Disinfectant Spray (Unsterilized)

TW: Hi-Life 消毒噴霧 (未滅菌)

Taiwan·Risk Class 1·TAIWAN STANCH CO., LTD.·Registered Apr 24, 2017 – Apr 24, 2022Cancelled

Registration details

Analysis ID: 4e6bea6c4dc3082cb8e89718b28b0cd8

Company information

Manufacturer: TAIWAN STANCH CO., LTD.
Manufacturer Country: Taiwan, Province of China
Authorized Representative: HI-LIFE INTERNATIONAL CO., LTD.

Product details

Intended Use: Limited to the first level identification scope of the Measures for the Administration of Medical Devices "Disinfectants for General Medical Devices (J.6890)".
Product Type (Level 1): J General hospital and personal use equipment
Product Type (Level 2): J.6890 Disinfectants for general medical equipment
Import Information: Domestic;; Contract manufacturing

Dates and status

Registration Date: Apr 24, 2017
Expiry Date: Apr 24, 2022
Cancellation Date: Apr 12, 2024

Cancellation information

Status: Logged out
Reason: 許可證已逾有效期

About this record

Access comprehensive regulatory information for Hi-Life Disinfectant Spray (Unsterilized) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number 4e6bea6c4dc3082cb8e89718b28b0cd8 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. 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.