Taiwan FDA registration d5143e093b180225f621da6be6796ec6

“Mediair” Trinity Resuscitator Set

TW: “上岳”三合一甦醒器

Taiwan·Risk Class 2·MD·Shangyue Technology Co., Ltd. Precision Factory·Registered Sep 01, 2021 – Sep 01, 2026Active

Registration details

Analysis ID: d5143e093b180225f621da6be6796ec6
License Form: Ministry of Health Medical Device Manufacturing No. 007245

Company information

Manufacturer: Shangyue Technology Co., Ltd. Precision Factory
Manufacturer Country: Taiwan, Province of China
Authorized Representative: EMG TECHNOLOGY CO., LTD.

Product details

Intended Use: Details are as detailed as approved Chinese instructions
Product Type (Level 1): D Devices for anesthesiology
Product Type (Level 2): D5925 Powered Emergency Respirator
Import Information: Produced in Taiwan, China

Dates and status

Registration Date: Sep 01, 2021
Expiry Date: Sep 01, 2026

About this record

Access comprehensive regulatory information for “Mediair” Trinity Resuscitator Set in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number d5143e093b180225f621da6be6796ec6 and manufactured by Shangyue Technology Co., Ltd. Precision Factory. The authorized representative in Taiwan is EMG TECHNOLOGY CO., LTD..

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