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“AirSep” VisionAire Oxygen Concentrator - Taiwan Registration 57eb126945bb86091d44854cb869396b

Access comprehensive regulatory information for “AirSep” VisionAire Oxygen Concentrator in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 57eb126945bb86091d44854cb869396b and manufactured by AIRSEP CORPORATION. The authorized representative in Taiwan is TAI CHI ENTERPRISE 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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57eb126945bb86091d44854cb869396b
Registration Details
Taiwan FDA Registration: 57eb126945bb86091d44854cb869396b
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Device Details

“AirSep” VisionAire Oxygen Concentrator
TW: “艾爾斯”夢幻型氧氣濃縮機
Risk Class 2
MD
Cancelled

Registration Details

57eb126945bb86091d44854cb869396b

Ministry of Health Medical Device Import No. 025218

DHA05602521804

Company Information

United States

Product Details

D Devices for anesthesiology

D5440 portable oxygen generator

Imported from abroad

Dates and Status

Aug 06, 2013

Aug 06, 2018

Aug 05, 2022

Cancellation Information

Logged out

未展延而逾期者