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"Japan Lai Fuen" Fix fixed bent electrode catheter - Taiwan Registration 69abf7c654a5cd724117f1b9e1ab069e

Access comprehensive regulatory information for "Japan Lai Fuen" Fix fixed bent 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 69abf7c654a5cd724117f1b9e1ab069e 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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69abf7c654a5cd724117f1b9e1ab069e
Registration Details
Taiwan FDA Registration: 69abf7c654a5cd724117f1b9e1ab069e
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Device Details

"Japan Lai Fuen" Fix fixed bent electrode catheter
TW: โ€œๆ—ฅๆœฌไพ†ๅฏŒๆฉโ€่ฒๅ…‹ๆ–ฏๅ›บๅฎšๅฝŽ้›ปๆฅตๅฐŽ็ฎก
Risk Class 2

Registration Details

69abf7c654a5cd724117f1b9e1ab069e

DHA00602293001

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

Nov 23, 2011

Nov 23, 2026