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"Kaiden" Matilyn Benda coronary artery dilator stent system - Taiwan Registration 7873d4307164a85909ed18f76fea7330

Access comprehensive regulatory information for "Kaiden" Matilyn Benda coronary artery dilator stent system in Taiwan's medical device market through Pure Global AI's free database. is registered under number 7873d4307164a85909ed18f76fea7330 and manufactured by GUIDANT IRELAND. 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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7873d4307164a85909ed18f76fea7330
Registration Details
Taiwan FDA Registration: 7873d4307164a85909ed18f76fea7330
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Device Details

"Kaiden" Matilyn Benda coronary artery dilator stent system
TW: "ๅ‡ฑ็™ป" ้ฆฌ่’‚็ณๅฅ”้”ๅ† ็‹€ๅ‹•่„ˆๆ“ดๅผตๆ”ฏๆžถ็ณป็ตฑ
Cancelled

Registration Details

7873d4307164a85909ed18f76fea7330

DHA00601010608

Company Information

Product Details

Vacuum.

E Cardiovascular Medicine Science

E.1310 ็ถ“็šฎๅฐŽ็ฎก็”จ่ก€็ฎกๆ“ดๅผตๅ™จ

import

Dates and Status

Oct 07, 2002

Oct 07, 2007

Nov 06, 2012

Cancellation Information

Logged out

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