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"Japan Lai Fuen" Ipita unidirectional electrode catheter - Taiwan Registration d73848b2a1b85c5542f4d331e40e9b17

Access comprehensive regulatory information for "Japan Lai Fuen" Ipita unidirectional 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 d73848b2a1b85c5542f4d331e40e9b17 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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d73848b2a1b85c5542f4d331e40e9b17
Registration Details
Taiwan FDA Registration: d73848b2a1b85c5542f4d331e40e9b17
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Device Details

"Japan Lai Fuen" Ipita unidirectional electrode catheter
TW: โ€œๆ—ฅๆœฌไพ†ๅฏŒๆฉโ€ๆ„็šฎๆ–ฏๅก”ๅ–ฎๅ‘้›ปๆฅตๅฐŽ็ฎก
Risk Class 2

Registration Details

d73848b2a1b85c5542f4d331e40e9b17

DHA00602283201

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

Oct 03, 2011

Oct 03, 2026