Taiwan FDA registration 4923221d637542a981768cc9638cd031

”Mediair” Oxygen Pressure Hose(Non-Sterile)

TW: “上岳” 氧氣壓力管(未滅菌)

Taiwan·Risk Class 1·MD·Shangyue Technology Co., Ltd. Precision Factory·Registered Apr 29, 2021 – Apr 29, 2026Expired

Registration details

Analysis ID: 4923221d637542a981768cc9638cd031
License Form: Ministry of Health Medical Device Manufacturing No. 009082

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: Limited to the first level identification range of pressure pipelines and their accessories (D.5860) of the management measures for medical equipment.
Product Type (Level 1): D Devices for anesthesiology
Product Type (Level 2): D5860 pressure lines and accessories
Import Information: Produced in Taiwan, China

Dates and status

Registration Date: Apr 29, 2021
Expiry Date: Apr 29, 2026

About this record

Access comprehensive regulatory information for ”Mediair” Oxygen Pressure Hose(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 4923221d637542a981768cc9638cd031 and manufactured by Shangyue Technology Co., Ltd. Precision Factory. The authorized representative in Taiwan is EMG TECHNOLOGY CO., LTD..

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