Taiwan FDA registration b7a40c96f1082731b5b7866b62fbc641
“Nihon Kohden” BEDSIDE MONITOR CSM-1000 Series Life Scope G
TW: “日本光電”床邊生理監視器
Taiwan·Risk Class 2·MD·Nihon Kohden Tomioka Corporation Tomioka Production Center·Registered Sep 06, 2017 – Sep 06, 2027ActiveRegistration details
- Analysis ID
- b7a40c96f1082731b5b7866b62fbc641
- License Form
- Ministry of Health Medical Device Import No. 030180
- Customs Code
- DHA05603018002
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 devices
- Product Type (Level 2)
- E2300 Cardiac Monitor (incl. Cardiac Counter and Heart Rate Alert)
- Import Information
- Imported from abroad
Dates and status
- Registration Date
- Sep 06, 2017
- Expiry Date
- Sep 06, 2027
About this record
Access comprehensive regulatory information for “Nihon Kohden” BEDSIDE MONITOR CSM-1000 Series Life Scope G in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number b7a40c96f1082731b5b7866b62fbc641 and manufactured by Nihon Kohden Tomioka Corporation Tomioka Production Center. The authorized representative in Taiwan is K&C MEDICAL CO., LTD..
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