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“Nihon Kohden” Automated External Defibrillator - Taiwan Registration 8e084ca6250aea5beab88b9693dfc8c8

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 8e084ca6250aea5beab88b9693dfc8c8 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, For spare parts system only;;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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8e084ca6250aea5beab88b9693dfc8c8
Registration Details
Taiwan FDA Registration: 8e084ca6250aea5beab88b9693dfc8c8
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Device Details

“Nihon Kohden” Automated External Defibrillator
TW: “日本光電”自動體外除顫器
Risk Class 3
MD

Registration Details

8e084ca6250aea5beab88b9693dfc8c8

Ministry of Health Medical Device Import No. 026405

DHA05602640508

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 17, 2014

Jul 17, 2024