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“Abbott” Gallant Implantable Cardioverter Defibrillator - Taiwan Registration 0b0412b2d4a45e1a69eaeec232fdd351

Access comprehensive regulatory information for “Abbott” Gallant 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 0b0412b2d4a45e1a69eaeec232fdd351 and manufactured by St. Jude Medical Operations (M) Sdn. Bhd.. 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 OPERATIONS (M) SDN. BHD., 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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0b0412b2d4a45e1a69eaeec232fdd351
Registration Details
Taiwan FDA Registration: 0b0412b2d4a45e1a69eaeec232fdd351
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Device Details

“Abbott” Gallant Implantable Cardioverter Defibrillator
TW: “雅培”給力植入式心律去顫器
Risk Class 3
MD

Registration Details

0b0412b2d4a45e1a69eaeec232fdd351

Ministry of Health Medical Device Import No. 034223

DHA05603422301

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

Dec 17, 2020

Dec 17, 2025

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