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“Uptake” InterVapor System - Taiwan Registration ff2b8e9ec2bb05598cc0f3fc65d72aae

Access comprehensive regulatory information for “Uptake” InterVapor System in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number ff2b8e9ec2bb05598cc0f3fc65d72aae and manufactured by Uptake Medical B.V.. The authorized representative in Taiwan is ERA BIOTEQ 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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ff2b8e9ec2bb05598cc0f3fc65d72aae
Registration Details
Taiwan FDA Registration: ff2b8e9ec2bb05598cc0f3fc65d72aae
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Device Details

“Uptake” InterVapor System
TW: “奧提克”支氣管鏡蒸氣治療系統
Risk Class 2
MD

Registration Details

ff2b8e9ec2bb05598cc0f3fc65d72aae

Ministry of Health Medical Device Import No. 033670

DHA05603367005

Company Information

Netherlands

Product Details

The InterVapor system is suitable for the treatment of patients with heterogeneous emphysema and hot water vapor therapy for the most severely ill lung segments to achieve bronchoscopic lung volume reduction.

G ENT device

G9999 Other

Imported from abroad

Dates and Status

Aug 06, 2020

Aug 06, 2025