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Temporary Rhythm Apparatus "Medtronic" - Taiwan Registration 2e4b1e8e9bdc032d3ba25d5afb829742

Access comprehensive regulatory information for Temporary Rhythm Apparatus "Medtronic" in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 3 medical device is registered under number 2e4b1e8e9bdc032d3ba25d5afb829742 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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2e4b1e8e9bdc032d3ba25d5afb829742
Registration Details
Taiwan FDA Registration: 2e4b1e8e9bdc032d3ba25d5afb829742
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Device Details

Temporary Rhythm Apparatus "Medtronic"
TW: ๆšซๆ™‚ๆ€ง็ฏ€ๅพ‹ๅ™จใ€€ใ€็พŽๆ•ฆๅŠ›ใ€ž
Risk Class 3
Cancelled

Registration Details

2e4b1e8e9bdc032d3ba25d5afb829742

DHA00600854901

Company Information

United States

Product Details

0609 Extracorporeal cardiac plasticist

import

Dates and Status

Feb 06, 1998

Feb 06, 2018

Dec 13, 2019

Cancellation Information

Logged out

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