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“Nihon Kohden” Cardiolife Defibrillator - Taiwan Registration dd81ee7d5631f659d78b92029a88f74e

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 dd81ee7d5631f659d78b92029a88f74e 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 Kawamoto Production Center, Nihon Kohden Tomioka Corporation Tomioka 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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Registration Details
Taiwan FDA Registration: dd81ee7d5631f659d78b92029a88f74e
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Device Details

“Nihon Kohden” Cardiolife Defibrillator
TW: “日本光電”心臟除顫器
Risk Class 3
MD

Registration Details

dd81ee7d5631f659d78b92029a88f74e

Ministry of Health Medical Device Import No. 028631

DHA05602863101

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

Jul 13, 2016

Jul 13, 2026

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