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“NIHON KOHDEN” Automated External Defibrillator - Taiwan Registration 2c291d32949b8710a1e9a9da86bc604a

Access comprehensive regulatory information for “NIHON KOHDEN” Automated External Defibrillator in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 3 medical device is registered under number 2c291d32949b8710a1e9a9da86bc604a and manufactured by For spare parts system only;;Nihon Kohden Tomioka Corporation Tomioka Production Center. The authorized representative in Taiwan is KWANG TEN TRADING CO., LTD..

This page provides complete technical specifications, regulatory compliance details, 1 companies making similar products including 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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2c291d32949b8710a1e9a9da86bc604a
Registration Details
Taiwan FDA Registration: 2c291d32949b8710a1e9a9da86bc604a
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Device Details

“NIHON KOHDEN” Automated External Defibrillator
TW: “日本光電”自動體外心臟電擊器
Risk Class 3
MD

Registration Details

2c291d32949b8710a1e9a9da86bc604a

Ministry of Health Medical Device Import No. 025825

DHA05602582502

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

Feb 27, 2014

Feb 27, 2024

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