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"Japan Lai Fuen" Sneak bidirectional electrode catheter - Taiwan Registration d60ad32dd48ce6d3bb2e76b7fe76188a

Access comprehensive regulatory information for "Japan Lai Fuen" Sneak bidirectional electrode catheter in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number d60ad32dd48ce6d3bb2e76b7fe76188a and manufactured by JAPAN LIFELINE CO., LTD.;; Japan Lifeline Co., Ltd. Toda 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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d60ad32dd48ce6d3bb2e76b7fe76188a
Registration Details
Taiwan FDA Registration: d60ad32dd48ce6d3bb2e76b7fe76188a
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Device Details

"Japan Lai Fuen" Sneak bidirectional electrode catheter
TW: โ€œๆ—ฅๆœฌไพ†ๅฏŒๆฉโ€ๅฒๅฅˆๅ…‹้›™ๅ‘้›ปๆฅตๅฐŽ็ฎก
Risk Class 2

Registration Details

d60ad32dd48ce6d3bb2e76b7fe76188a

DHA00602294603

Product Details

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

E Cardiovascular Medicine Science

E.1220 ้›ปๆฅต่จ˜้Œ„ๅฐŽ็ฎกๆˆ–้›ปๆฅต่จ˜้Œ„ๆŽข้ ญ

import

Dates and Status

Dec 01, 2011

Dec 01, 2026