Taiwan FDA registration 2d5f6951252ff8e068e9c85bf184dc92

"Yaohong" non-powered treatment mattress (unsterilized)　　

TW: “耀宏”非動力式治療床墊 (未滅菌)　　

Taiwan·Risk Class 1·YAO HONG INSTRUMENT PLANT CO., LTD.·Registered Nov 25, 2010 – Nov 25, 2025Cancelled

Registration details

Analysis ID: 2d5f6951252ff8e068e9c85bf184dc92

Company information

Manufacturer: YAO HONG INSTRUMENT PLANT CO., LTD.
Manufacturer Country: Taiwan, Province of China
Authorized Representative: YAO HONG INSTRUMENT PLANT CO., LTD.

Product details

Intended Use: Limited to the first level identification scope of the Measures for the Administration of Medical Devices "Non-powered Therapeutic Mattresses (J.5150)".
Product Type (Level 1): J General hospital and personal use equipment
Product Type (Level 2): J.5150 Non-powered floating therapy mattress
Import Information: Domestic

Dates and status

Registration Date: Nov 25, 2010
Expiry Date: Nov 25, 2025
Cancellation Date: Sep 30, 2021

Cancellation information

Status: Logged out
Reason: 轉為登錄字號

About this record

Access comprehensive regulatory information for "Yaohong" non-powered treatment mattress (unsterilized)　　 in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number 2d5f6951252ff8e068e9c85bf184dc92 and manufactured by YAO HONG INSTRUMENT PLANT CO., LTD.. The authorized representative in Taiwan is YAO HONG INSTRUMENT PLANT 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.