Taiwan FDA registration 5f3f6a34d7e6b650706642f3ef23a094

"Yaohong" Patient Lifting Device (Unsterilized)

TW: "耀宏" 病患移位裝置 (未滅菌)

Taiwan·Risk Class 1·YAO HONG INSTRUMENT PLANT CO., LTD.·Registered Nov 10, 2015 – Nov 10, 2025Cancelled

Registration details

Analysis ID: 5f3f6a34d7e6b650706642f3ef23a094

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): J.6785 Manual Patient Conveying Device
Import Information: Domestic

Dates and status

Registration Date: Nov 10, 2015
Expiry Date: Nov 10, 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" Patient Lifting 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 5f3f6a34d7e6b650706642f3ef23a094 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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