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“Vyaire” Pulmonary Function Test System - Taiwan Registration 9e46feb14f981f9b7164ed0e61203f79

Access comprehensive regulatory information for “Vyaire” Pulmonary Function Test System in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 9e46feb14f981f9b7164ed0e61203f79 and manufactured by Vyaire Medical GmbH. The authorized representative in Taiwan is BIOSYSTEMS INC..

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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9e46feb14f981f9b7164ed0e61203f79
Registration Details
Taiwan FDA Registration: 9e46feb14f981f9b7164ed0e61203f79
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Device Details

“Vyaire” Pulmonary Function Test System
TW: “維亞爾” 肺功能測試系統
Risk Class 2
MD

Registration Details

9e46feb14f981f9b7164ed0e61203f79

Ministry of Health Medical Device Import No. 034478

DHA05603447805

Company Information

Germany

Product Details

For details, it is Chinese approved copy of the imitation order

D Devices for anesthesiology

D1840 Spirometer for diagnosis

Imported from abroad

Dates and Status

Mar 30, 2021

Mar 30, 2026