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"Medtronic" Pulse Optimization Pulse Ablation Instrument and Components - Taiwan Registration 693675b63c11bef524d7b5c3ba2c82de

Access comprehensive regulatory information for "Medtronic" Pulse Optimization Pulse Ablation Instrument and Components in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 3 medical device is registered under number 693675b63c11bef524d7b5c3ba2c82de and manufactured by Medtronic Inc.. The authorized representative in Taiwan is MEDTRONIC (TAIWAN) LTD..

This page provides complete technical specifications, regulatory compliance details. 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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693675b63c11bef524d7b5c3ba2c82de
Registration Details
Taiwan FDA Registration: 693675b63c11bef524d7b5c3ba2c82de
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Device Details

"Medtronic" Pulse Optimization Pulse Ablation Instrument and Components
TW: โ€œ็พŽๆ•ฆๅŠ›โ€ ่„ˆๅ„ช้ธ่„ˆ่กๆถˆ่žๅ„€ๅŠ็ต„ไปถ
Risk Class 3

Registration Details

693675b63c11bef524d7b5c3ba2c82de

DHA05603727404

Company Information

United States

Product Details

Details are as detailed as approved Chinese instructions

E Cardiovascular Medicine Science

E.0008.

import

Dates and Status

Aug 11, 2024

Aug 11, 2029