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"Asahi Dofan balloon expansion catheter - Taiwan Registration 468b08b73d9616640c7f2ef089a3e335

Access comprehensive regulatory information for "Asahi Dofan balloon expansion catheter in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 3 medical device is registered under number 468b08b73d9616640c7f2ef089a3e335 and manufactured by ASAHI INTECC CO., LTD. SETO FACTORY. The authorized representative in Taiwan is QUALTECH CONSULTING CORPORATION.

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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468b08b73d9616640c7f2ef089a3e335
Registration Details
Taiwan FDA Registration: 468b08b73d9616640c7f2ef089a3e335
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Device Details

"Asahi Dofan balloon expansion catheter
TW: โ€œๆœๆ—ฅโ€ๆœตๅ‡กๆฐฃ็ƒๆ“ดๅผตๅฐŽ็ฎก
Risk Class 3
Cancelled

Registration Details

468b08b73d9616640c7f2ef089a3e335

DHA00602206701

Company Information

Product Details

This product has a dilated effect on narrowed coronary arteries during balloon dilation (PTCA) and provides dilation after positioning stents

E Cardiovascular Medicine Science

E.0005.

import

Dates and Status

Feb 23, 2011

Feb 23, 2021

Sep 08, 2023

Cancellation Information

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