Taiwan FDA registration e48ffb0e841c016eaeb7dce7ebd677f9
"Nippon Opto" cardiopulmonary resuscitation guide
TW: “日本光電”心肺復甦指引器
Taiwan·Risk Class 3·Nihon Kohden Tomioka Corporation Tomioka Production Center;; NIHON KOHDEN CORPORATION·Registered Sep 20, 2017 – Sep 20, 2027ActiveRegistration details
- Analysis ID
- e48ffb0e841c016eaeb7dce7ebd677f9
- Customs Code
- DHA05603025402
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.5200 體外心臟加壓器
- Import Information
- import
Dates and status
- Registration Date
- Sep 20, 2017
- Expiry Date
- Sep 20, 2027
About this record
Access comprehensive regulatory information for "Nippon Opto" cardiopulmonary resuscitation guide in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 3 medical device is registered under number e48ffb0e841c016eaeb7dce7ebd677f9 and manufactured by Nihon Kohden Tomioka Corporation Tomioka Production Center;; NIHON KOHDEN CORPORATION. The authorized representative in Taiwan is K&C MEDICAL CO., LTD..
This page provides complete technical specifications, regulatory compliance details. 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.
Free DatabasePowered by Pure Global AI89,000+ Devices