Taiwan FDA registration dd81ee7d5631f659d78b92029a88f74e

“Nihon Kohden” Cardiolife Defibrillator

TW: “日本光電”心臟除顫器
Taiwan flagTaiwan·Risk Class 3·MD·Nihon Kohden Tomioka Corporation Tomioka Production Center·Registered Jul 13, 2016 – Jul 13, 2026Expired
Registration details
Analysis ID
dd81ee7d5631f659d78b92029a88f74e
License Form
Ministry of Health Medical Device Import No. 028631
Customs Code
DHA05602863101
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 13, 2016
Expiry Date
Jul 13, 2026
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About this record

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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