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”Mediair” Oxygen Pressure Hose(Non-Sterile) - Taiwan Registration 4923221d637542a981768cc9638cd031

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..

This page provides complete technical specifications, regulatory compliance details. Pure Global AI offers free access to 89,000+ Taiwan medical device registrations, helping global MedTech companies navigate Taiwan FDA regulations, identify competitors, and discover partnership opportunities efficiently.

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4923221d637542a981768cc9638cd031
Registration Details
Taiwan FDA Registration: 4923221d637542a981768cc9638cd031
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Device Details

”Mediair” Oxygen Pressure Hose(Non-Sterile)
TW: “上岳” 氧氣壓力管(未滅菌)
Risk Class 1
MD

Registration Details

4923221d637542a981768cc9638cd031

Ministry of Health Medical Device Manufacturing No. 009082

Company Information

Taiwan, Province of China

Product Details

Limited to the first level identification range of pressure pipelines and their accessories (D.5860) of the management measures for medical equipment.

D Devices for anesthesiology

D5860 pressure lines and accessories

Produced in Taiwan, China

Dates and Status

Apr 29, 2021

Apr 29, 2026