Taiwan FDA registration 9353fb62810a636c12390bf5d74c8874

“Yao-Hong”Moist heat pack (Non-Sterile)

TW: “耀宏”醫療用濕熱敷包（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: 9353fb62810a636c12390bf5d74c8874
License Form: Ministry of Health Medical Device Manufacturing Registration No. 003294

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 "Medical Hot and Humid Compress Packs (O.5730)".
Product Type (Level 1): o Equipment for physical medicine
Product Type (Level 2): O5730 Thermal and moist compress for medical use
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”Moist heat pack (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 9353fb62810a636c12390bf5d74c8874 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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