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“AirSep” NewLife Oxygen Concentrator - Taiwan Registration 35993f10be86ba614ec9eab35ca452bc

Access comprehensive regulatory information for “AirSep” NewLife 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 35993f10be86ba614ec9eab35ca452bc 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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35993f10be86ba614ec9eab35ca452bc
Registration Details
Taiwan FDA Registration: 35993f10be86ba614ec9eab35ca452bc
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Device Details

“AirSep” NewLife Oxygen Concentrator
TW: “艾爾斯” 新生型氧氣濃縮機
Risk Class 2
MD
Cancelled

Registration Details

35993f10be86ba614ec9eab35ca452bc

Ministry of Health Medical Device Import No. 025245

DHA05602524507

Company Information

United States

Product Details

D Devices for anesthesiology

D5440 portable oxygen generator

Imported from abroad

Dates and Status

Sep 24, 2013

Sep 24, 2018

Aug 05, 2022

Cancellation Information

Logged out

未展延而逾期者