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Edwards INSPIRIS RESILIA Aortic Valve - Taiwan Registration 7e2e89d86f0a6450baa550a829f4242e

Access comprehensive regulatory information for Edwards INSPIRIS RESILIA Aortic Valve in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 3 medical device is registered under number 7e2e89d86f0a6450baa550a829f4242e 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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7e2e89d86f0a6450baa550a829f4242e
Registration Details
Taiwan FDA Registration: 7e2e89d86f0a6450baa550a829f4242e
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Device Details

Edwards INSPIRIS RESILIA Aortic Valve
TW: ๆ„›ๅพท่ฏๆ€ก็‘ž่ฉฉไนพๅผ็“ฃ่†œ
Risk Class 3
MD

Registration Details

7e2e89d86f0a6450baa550a829f4242e

Ministry of Health Medical Device Import No. 031611

DHA05603161105

Company Information

United States

Product Details

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

E Cardiovascular devices

E3925 Heart valve replacement

Imported from abroad

Dates and Status

Apr 30, 2019

Apr 30, 2024