“Nihon Kohden” Cardiolife Defibrillator - Taiwan Registration a5cec8b65f23b6a2efd2f548b573c2cf
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 a5cec8b65f23b6a2efd2f548b573c2cf 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, Nihon Kohden Kawamoto 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
a5cec8b65f23b6a2efd2f548b573c2cf
Ministry of Health Medical Device Import No. 031201
DHA05603120102
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
Jun 26, 2018
Jun 26, 2028
“Nihon Kohden” Cardiolife Defibrillator Pads
Nihon Kohden Kawamoto Production Center
70d240f6d8d49b7ae4d167cdd27db6fd
2
“Nihon Kohden” Cardiolife Defibrillator
Nihon Kohden Tomioka Corporation Tomioka Production Center
dd81ee7d5631f659d78b92029a88f74e
3

