Taiwan FDA registration a381f9db322a5af2a9c3ab4355280203

"Hongxiang" pressure supply device (unsterilized)

TW: “鴻祥” 壓力供應裝置 (未滅菌)

Taiwan·Risk Class 1·HONG SHIANG TECHNOLOGY CO., LTD.·Registered Nov 07, 2012 – Nov 07, 2027Active

Registration details

Analysis ID: a381f9db322a5af2a9c3ab4355280203

Company information

Manufacturer: HONG SHIANG TECHNOLOGY CO., LTD.
Manufacturer Country: Taiwan, Province of China
Authorized Representative: HONG SHIANG TECHNOLOGY CO., LTD.

Product details

Intended Use: It is limited to the scope of first-class identification of the "Pressure Supply Device (O.5765)" of the Administrative Measures for the Classification and Classification of Medical Devices.
Product Type (Level 1): o Physical Medical Sciences
Product Type (Level 2): O.5765 壓力供應裝置
Import Information: Domestic

Dates and status

Registration Date: Nov 07, 2012
Expiry Date: Nov 07, 2027

About this record

Access comprehensive regulatory information for "Hongxiang" pressure supply device (unsterilized) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number a381f9db322a5af2a9c3ab4355280203 and manufactured by HONG SHIANG TECHNOLOGY CO., LTD.. The authorized representative in Taiwan is HONG SHIANG TECHNOLOGY 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.