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“Nihon Kohden” BEDSIDE MONITOR CSM-1000 Series Life Scope G - Taiwan Registration b7a40c96f1082731b5b7866b62fbc641

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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b7a40c96f1082731b5b7866b62fbc641
Registration Details
Taiwan FDA Registration: b7a40c96f1082731b5b7866b62fbc641
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Device Details

“Nihon Kohden” BEDSIDE MONITOR CSM-1000 Series Life Scope G
TW: “日本光電”床邊生理監視器
Risk Class 2
MD

Registration Details

b7a40c96f1082731b5b7866b62fbc641

Ministry of Health Medical Device Import No. 030180

DHA05603018002

Company Information

Product Details

For details, it is Chinese approved copy of the imitation order

E Cardiovascular devices

E2300 Cardiac Monitor (incl. Cardiac Counter and Heart Rate Alert)

Imported from abroad

Dates and Status

Sep 06, 2017

Sep 06, 2027