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“Edwards” HemoSphere Advanced Monitoring Platform - Taiwan Registration ab35f14000f6af3b1aa2024c6e2c6982

Access comprehensive regulatory information for “Edwards” HemoSphere Advanced Monitoring Platform in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number ab35f14000f6af3b1aa2024c6e2c6982 and manufactured by EDWARDS LIFESCIENCES LLC. The authorized representative in Taiwan is EDWARDS LIFESCIENCES (TAIWAN) CORPORATION.

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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ab35f14000f6af3b1aa2024c6e2c6982
Registration Details
Taiwan FDA Registration: ab35f14000f6af3b1aa2024c6e2c6982
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Device Details

“Edwards” HemoSphere Advanced Monitoring Platform
TW: “愛德華”希摩斯菲爾進階生理參數監測平台
Risk Class 2
MD

Registration Details

ab35f14000f6af3b1aa2024c6e2c6982

Ministry of Health Medical Device Import No. 030609

DHA05603060900

Company Information

United States

Product Details

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

E Cardiovascular devices

E1425 Programmable diagnostic PC

Imported from abroad

Dates and Status

Dec 07, 2017

Dec 07, 2027