Taiwan FDA registration 73558f7fde6c4eb19b3ae28520d58daf

“SJM” Fortify Assura Implantable Cardioverter Defibrillator

TW: “聖猷達”幅地法亞速拉植入式心律去顫器
Taiwan flagTaiwan·Risk Class 3·MD·ST. JUDE MEDICAL OPERATIONS (M) SDN. BHD.·Registered May 27, 2014 – May 27, 2019Cancelled
Registration details
Analysis ID
73558f7fde6c4eb19b3ae28520d58daf
License Form
Ministry of Health Medical Device Import No. 026218
Customs Code
DHA05602621809
Company information
Manufacturer Country
Malaysia
Authorized Representative
Abbott Medical Taiwan Co.
Product details
Product Type (Level 1)
E Cardiovascular devices
Product Type (Level 2)
E3610 Pulse generator for implantable heart rhythm apparatus
Import Information
Imported from abroad
Dates and status
Registration Date
May 27, 2014
Expiry Date
May 27, 2019
Cancellation Date
Jul 15, 2022
Cancellation information
Status
Logged out
Reason
未展延而逾期者
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About this record

Access comprehensive regulatory information for “SJM” Fortify Assura 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 73558f7fde6c4eb19b3ae28520d58daf 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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