Taiwan FDA registration 86dcf2a3676953ec60761420973c916a

"Yao-Hong" Plinth (Non-Sterile)

TW: "耀宏" 治療檯 (未滅菌)

Taiwan·Risk Class 1·MD·YAO HONG INSTRUMENT PLANT CO., LTD.·Registered Oct 01, 2021 – Oct 31, 2025Expired

Registration details

Analysis ID: 86dcf2a3676953ec60761420973c916a
License Form: Ministry of Health Medical Device Manufacturing Registration No. 003131

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 range of the Measures for the Administration of Medical Equipment "Treatment Table (O.3520)".
Product Type (Level 1): o Equipment for physical medicine
Product Type (Level 2): O3520 treatment unit
Import Information: Produced in Taiwan, China

Dates and status

Registration Date: Oct 01, 2021
Expiry Date: Oct 31, 2025

About this record

Access comprehensive regulatory information for "Yao-Hong" Plinth (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 86dcf2a3676953ec60761420973c916a 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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