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“SJM” Quadra Assura MP Implantable Cardioverter Defibrillator - Taiwan Registration 8acee977cfeb019d0968b32d9c995fa6

Access comprehensive regulatory information for “SJM” Quadra Assura MP 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 8acee977cfeb019d0968b32d9c995fa6 and manufactured by St. Jude Medical Cardiac Rhythm Management Division;;St. Jude Medical Puerto Rico, LLC. The authorized representative in Taiwan is Abbott Medical Taiwan Co..

This page provides complete technical specifications, regulatory compliance details, 2 companies making similar products including ST. JUDE MEDICAL OPERATIONS (M) SDN. BHD., St. Jude Medical, Cardiac Rhythm Management Division, and 2 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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8acee977cfeb019d0968b32d9c995fa6
Registration Details
Taiwan FDA Registration: 8acee977cfeb019d0968b32d9c995fa6
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Device Details

“SJM” Quadra Assura MP Implantable Cardioverter Defibrillator
TW: “聖猷達”克卓亞速拉多點式植入式心律去顫器
Risk Class 3
MD

Registration Details

8acee977cfeb019d0968b32d9c995fa6

Ministry of Health Medical Device Import No. 027278

DHA05602727806

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 30, 2015

Apr 30, 2025

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