“NIHON KOHDEN” Automated External Defibrillator
Taiwan·Risk Class 3·MD·For spare parts system only;;Nihon Kohden Tomioka Corporation Tomioka Production Center·Registered Feb 27, 2014 – Feb 27, 2024Expired- Analysis ID
- 2c291d32949b8710a1e9a9da86bc604a
- License Form
- Ministry of Health Medical Device Import No. 025825
- Customs Code
- DHA05602582502
- Manufacturer Country
- Japan;;United States
- Authorized Representative
- KWANG TEN TRADING CO., LTD.
- 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
- Registration Date
- Feb 27, 2014
- Expiry Date
- Feb 27, 2024
Top companies providing products similar to "“NIHON KOHDEN” Automated External Defibrillator"
Recently registered similar products
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 2c291d32949b8710a1e9a9da86bc604a and manufactured by For spare parts system only;;Nihon Kohden Tomioka Corporation Tomioka Production Center. The authorized representative in Taiwan is KWANG TEN TRADING CO., LTD..
This page provides complete technical specifications, regulatory compliance details, 1 companies making similar products including 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.