Taiwan FDA registration 4fd56934f8e7d0bcb6b1a96a093f43a3

"Yao-Hong" patient transfer device (Non-Sterile)

TW: "耀宏" 病患移位裝置 (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: 4fd56934f8e7d0bcb6b1a96a093f43a3
License Form: Ministry of Health Medical Device Manufacturing Registration No. 005936

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 of identification scope of the Measures for the Administration of Medical Devices "Manual Patient Transport Device (J.6785)".
Product Type (Level 1): J General hospital and personal use equipment
Product Type (Level 2): J6785 Manual Patient Conveyor
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" patient transfer device (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 4fd56934f8e7d0bcb6b1a96a093f43a3 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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