Taiwan FDA registration 8a0b178d51ecbfbbe9a17878d96b69d8

“Yao-Hong” Nonpowered Flotation Therapy Mattress(Non-Sterile)　　

TW: “耀宏”非動力式治療床墊 (未滅菌)　　

Taiwan·Risk Class 1·MD·YAO HONG INSTRUMENT PLANT CO., LTD.·Registered Oct 01, 2021 – Oct 31, 2026Active

Registration details

Analysis ID: 8a0b178d51ecbfbbe9a17878d96b69d8
License Form: Ministry of Health Medical Device Manufacturing Registration No. 003212

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): J5150 Non-powered treatment mattress
Import Information: Produced in Taiwan, China

Dates and status

Registration Date: Oct 01, 2021
Expiry Date: Oct 31, 2026

About this record

Access comprehensive regulatory information for “Yao-Hong” Nonpowered Flotation Therapy Mattress(Non-Sterile)　　 in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number 8a0b178d51ecbfbbe9a17878d96b69d8 and manufactured by YAO HONG INSTRUMENT PLANT CO., LTD.. The authorized representative in Taiwan is YAO HONG INSTRUMENT PLANT CO., LTD..

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