Taiwan FDA registration 8e084ca6250aea5beab88b9693dfc8c8

“Nihon Kohden” Automated External Defibrillator

TW: “日本光電”自動體外除顫器
Taiwan flagTaiwan·Risk Class 3·MD·Nihon Kohden Tomioka Corporation Tomioka Production Center·Registered Jul 17, 2014 – Jul 17, 2024Expired
Registration details
Analysis ID
8e084ca6250aea5beab88b9693dfc8c8
License Form
Ministry of Health Medical Device Import No. 026405
Customs Code
DHA05602640508
Company information
Manufacturer Country
Japan
Authorized Representative
K&C MEDICAL CO., LTD.
Product details
Intended Use
For details, it is Chinese approved copy of the imitation order
Product Type (Level 1)
E Cardiovascular devices
Product Type (Level 2)
E5310 Automated External Defibrillator
Import Information
Imported from abroad
Dates and status
Registration Date
Jul 17, 2014
Expiry Date
Jul 17, 2024
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About this record

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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