“Nihon Kohden” Cardiolife Defibrillator
- Analysis ID
- dd81ee7d5631f659d78b92029a88f74e
- License Form
- Ministry of Health Medical Device Import No. 028631
- Customs Code
- DHA05602863101
- Manufacturer Country
- Japan
- Authorized Representative
- K&C MEDICAL 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
- Jul 13, 2016
- Expiry Date
- Jul 13, 2026
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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.