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"Abbott" coronary artery dilation stent system - Taiwan Registration 23405cef262fb9958d06e4e17568cd18

Access comprehensive regulatory information for "Abbott" coronary artery dilation stent system in Taiwan's medical device market through Pure Global AI's free database. is registered under number 23405cef262fb9958d06e4e17568cd18 and manufactured by ABBOTT VASCULAR. The authorized representative in Taiwan is ABBOTT LABORATORIES SERVICES LLC TAIWAN BRANCH (U.S.A.).

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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23405cef262fb9958d06e4e17568cd18
Registration Details
Taiwan FDA Registration: 23405cef262fb9958d06e4e17568cd18
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Device Details

"Abbott" coronary artery dilation stent system
TW: "ไบžๅŸน"ๅ† ็‹€ๅ‹•่„ˆๆ“ดๅผตๆ”ฏๆžถ็ณป็ตฑ
Cancelled

Registration Details

23405cef262fb9958d06e4e17568cd18

DHA00600892806

Company Information

United States

Product Details

0399 Other artificial function substitutes

import

Dates and Status

Nov 17, 1998

Nov 17, 2013

Sep 26, 2016

Cancellation Information

Logged out

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