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"Asahi Uyouke angiography wire" - Taiwan Registration d2cc585707f1b0850a67280488c59563

Access comprehensive regulatory information for "Asahi Uyouke angiography wire" in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number d2cc585707f1b0850a67280488c59563 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, 2 companies making similar products including ASAHI INTECC(THAILAND) CO.,LTD, ASAHI INTECC CO., LTD.;; Asahi Intecc Hanoi Co., Ltd., and 2 recent registrations in the same category. 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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d2cc585707f1b0850a67280488c59563
Registration Details
Taiwan FDA Registration: d2cc585707f1b0850a67280488c59563
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Device Details

"Asahi Uyouke angiography wire"
TW: "ๆœๆ—ฅ"ๅ„ชไฝ ๅฎข่ก€็ฎก้€ ๅฝฑๅฐŽ็ทš
Risk Class 2
Cancelled

Registration Details

d2cc585707f1b0850a67280488c59563

DHA00601702402

Company Information

Product Details

For details, it is Chinese approved copy of the imitation order

E Cardiovascular Medicine Science

E.1330 Catheter Guide Wires

import

Dates and Status

Aug 21, 2006

Aug 21, 2021

Sep 08, 2023

Cancellation Information

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