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“SJM” Ellipse Implantable Cardioverter Defibrillator - Taiwan Registration e4cf4a16e6e034e5fbe24c3a6dd0feef

Access comprehensive regulatory information for “SJM” Ellipse Implantable Cardioverter Defibrillator in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 3 medical device is registered under number e4cf4a16e6e034e5fbe24c3a6dd0feef and manufactured by ST. JUDE MEDICAL CARDIAC RHYTHM MANAGEMENT DIVISION. The authorized representative in Taiwan is Abbott Medical Taiwan Co..

This page provides complete technical specifications, regulatory compliance details, 1 companies making similar products including St. Jude Medical Cardiac Rhythm Management Division;;St. Jude Medical Puerto Rico, LLC, 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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e4cf4a16e6e034e5fbe24c3a6dd0feef
Registration Details
Taiwan FDA Registration: e4cf4a16e6e034e5fbe24c3a6dd0feef
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Device Details

“SJM” Ellipse Implantable Cardioverter Defibrillator
TW: “聖猷達”依利普植入式心律去顫器
Risk Class 3
MD

Registration Details

e4cf4a16e6e034e5fbe24c3a6dd0feef

Ministry of Health Medical Device Import No. 030816

DHA05603081605

Company Information

Product Details

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

E Cardiovascular devices

E3610 Pulse generator for implantable heart rhythm apparatus

Imported from abroad

Dates and Status

Apr 23, 2018

Apr 23, 2028

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