“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.
Device Details
Registration Details
8e084ca6250aea5beab88b9693dfc8c8
Ministry of Health Medical Device Import No. 026405
DHA05602640508
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
“Nihon Kohden” Automated External Defibrillator AED-3100 cardiolife AED
Nihon Kohden Tomioka Corporation Tomioka Production Center
fca619b4856988b4756bdc7547864baa
3
“NIHON KOHDEN” Automated External Defibrillator
For spare parts system only;;Nihon Kohden Tomioka Corporation Tomioka Production Center
2c291d32949b8710a1e9a9da86bc604a
3

