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“Nihon Kohden” Cardiolife Defibrillator - Taiwan Registration a5cec8b65f23b6a2efd2f548b573c2cf

Access comprehensive regulatory information for “Nihon Kohden” Cardiolife Defibrillator in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 3 medical device is registered under number a5cec8b65f23b6a2efd2f548b573c2cf and manufactured by Nihon Kohden Tomioka Corporation Tomioka Production Center. The authorized representative in Taiwan is K&C MEDICAL CO., LTD..

This page provides complete technical specifications, regulatory compliance details, 2 companies making similar products including Nihon Kohden Tomioka Corporation Tomioka Production Center, Nihon Kohden Kawamoto Production Center, 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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a5cec8b65f23b6a2efd2f548b573c2cf
Registration Details
Taiwan FDA Registration: a5cec8b65f23b6a2efd2f548b573c2cf
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Device Details

“Nihon Kohden” Cardiolife Defibrillator
TW: “日本光電”心臟電擊器
Risk Class 3
MD

Registration Details

a5cec8b65f23b6a2efd2f548b573c2cf

Ministry of Health Medical Device Import No. 031201

DHA05603120102

Company Information

Product Details

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

E Cardiovascular devices

E5310 Automated External Defibrillator

Imported from abroad

Dates and Status

Jun 26, 2018

Jun 26, 2028

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