“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.
Device Details
Registration Details
dd81ee7d5631f659d78b92029a88f74e
Ministry of Health Medical Device Import No. 028631
DHA05602863101
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
“Nihon Kohden” Cardiolife Defibrillator
Nihon Kohden Tomioka Corporation Tomioka Production Center
a5cec8b65f23b6a2efd2f548b573c2cf
3
“Nihon Kohden” Cardiolife Defibrillator Pads
Nihon Kohden Kawamoto Production Center
70d240f6d8d49b7ae4d167cdd27db6fd
2

