Taiwan FDA registration fe3d183bb44a7f9a721b1f0552b300bd
“SJM” Quadra Allure MP Cardiac Resynchronization Therapy Pulse Generator
TW: “聖猷達”克卓亞絡多點式心臟節律器
Taiwan·Risk Class 3·MD·ST. JUDE MEDICAL CARDIAC RHYTHM MANAGEMENT DIVISION·Registered Mar 06, 2019 – Mar 06, 2024ExpiredRegistration details
- Analysis ID
- fe3d183bb44a7f9a721b1f0552b300bd
- License Form
- Ministry of Health Medical Device Import No. 032282
- Customs Code
- DHA05603228204
Company information
- Manufacturer Country
- United States
- Authorized Representative
- Abbott Medical Taiwan Co.
Product details
- Intended Use
- For details, it is Chinese approved copy of the imitation order
- 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
- Mar 06, 2019
- Expiry Date
- Mar 06, 2024
About this record
Access comprehensive regulatory information for “SJM” Quadra Allure MP Cardiac Resynchronization Therapy Pulse Generator in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 3 medical device is registered under number fe3d183bb44a7f9a721b1f0552b300bd and manufactured by ST. JUDE MEDICAL CARDIAC RHYTHM MANAGEMENT DIVISION. The authorized representative in Taiwan is Abbott Medical Taiwan Co..
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