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"Japan to Fuen" Aislitwiza guide - Taiwan Registration 17ea812f65763d21c9c9a15711ce5529

Access comprehensive regulatory information for "Japan to Fuen" Aislitwiza guide in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 17ea812f65763d21c9c9a15711ce5529 and manufactured by JAPAN LIFELINE CO., LTD.;; Japan Lifeline Co., Ltd. Toda Factory. The authorized representative in Taiwan is ZENITH INC..

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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17ea812f65763d21c9c9a15711ce5529
Registration Details
Taiwan FDA Registration: 17ea812f65763d21c9c9a15711ce5529
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Device Details

"Japan to Fuen" Aislitwiza guide
TW: โ€œๆ—ฅๆœฌไพ†ๅฏŒๆฉโ€่‰พๆ–ฏๅˆฉ็‰นๅจๆœญๅฐŽๅผ•็ทš
Risk Class 2
Cancelled

Registration Details

17ea812f65763d21c9c9a15711ce5529

DHA00602282402

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

Sep 27, 2011

Sep 27, 2021

Aug 23, 2023

Cancellation Information

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