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“Beurer”Pulse Oximeter - Taiwan Registration f4fe0d255a700faf7422cc1eff44ff86

Access comprehensive regulatory information for “Beurer”Pulse Oximeter in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number f4fe0d255a700faf7422cc1eff44ff86 and manufactured by Beurer GmbH. The authorized representative in Taiwan is BIOWELL HEALTH & WELL-BEING 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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f4fe0d255a700faf7422cc1eff44ff86
Registration Details
Taiwan FDA Registration: f4fe0d255a700faf7422cc1eff44ff86
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Device Details

“Beurer”Pulse Oximeter
TW: “德國博依”血氧濃度計
Risk Class 2
MD

Registration Details

f4fe0d255a700faf7422cc1eff44ff86

Ministry of Health Medical Device Import No. 035320

DHA05603532001

Company Information

Germany

Product Details

Details are as detailed as approved Chinese instructions

E Cardiovascular Medicine Science

E2700 Oximeter

Imported from abroad

Dates and Status

Mar 09, 2022

Mar 09, 2027