Taiwan FDA registration 6d5844a56c2f7836af9bcef84347bb1a
"Nippon Optoelectronics" defibrillator system
TW: “日本光電”去顫器系統
Taiwan·Risk Class 3·Nihon Kohden Tomioka Corporation Tomioka Production Center;; NIHON KOHDEN CORPORATION·Registered Sep 26, 2020 – Sep 26, 2025ExpiredRegistration details
- Analysis ID
- 6d5844a56c2f7836af9bcef84347bb1a
- Customs Code
- DHA05603396600
Company information
- Manufacturer Country
- Japan
- Authorized Representative
- K&C MEDICAL CO., LTD.
Product details
- Intended Use
- For details, it is Chinese approved copy of the imitation order
- Product Type (Level 1)
- E Cardiovascular Medicine Science
- Product Type (Level 2)
- E.5310 自動體外去顫器系統
- Import Information
- import
Dates and status
- Registration Date
- Sep 26, 2020
- Expiry Date
- Sep 26, 2025
About this record
Access comprehensive regulatory information for "Nippon Optoelectronics" defibrillator system in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 3 medical device is registered under number 6d5844a56c2f7836af9bcef84347bb1a and manufactured by Nihon Kohden Tomioka Corporation Tomioka Production Center;; NIHON KOHDEN CORPORATION. The authorized representative in Taiwan is K&C MEDICAL CO., LTD..
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