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“Vyaire”Spirometer - Taiwan Registration 798d92c072292de303d40a355d51ba40

Access comprehensive regulatory information for “Vyaire”Spirometer in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 798d92c072292de303d40a355d51ba40 and manufactured by Vyaire Medical GmbH. The authorized representative in Taiwan is BIOSYSTEMS INC..

This page provides complete technical specifications, regulatory compliance details, 1 companies making similar products including Vyaire Medical GmbH, and 1 recent registrations in the same category. 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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798d92c072292de303d40a355d51ba40
Registration Details
Taiwan FDA Registration: 798d92c072292de303d40a355d51ba40
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Device Details

“Vyaire”Spirometer
TW: “維亞爾”肺量計
Risk Class 2
MD

Registration Details

798d92c072292de303d40a355d51ba40

Ministry of Health Medical Device Import No. 035534

DHA05603553407

Company Information

Germany

Product Details

Details are as detailed as approved Chinese instructions

D Anesthesiology

D1840 Spirometer for diagnosis

Imported from abroad

Dates and Status

Jul 22, 2022

Jul 22, 2027

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