Taiwan FDA registration ffe72fc6ee6c09392912cccb5d4c2963

"Nippon Opto" bedside monitor

TW: “日本光電”床邊監視器
Taiwan flagTaiwan·Risk Class 2·Nihon Kohden Tomioka Corporation Tomioka Production Center·Registered Sep 02, 2015 – Sep 02, 2025Expired
Registration details
Analysis ID
ffe72fc6ee6c09392912cccb5d4c2963
Customs Code
DHA05602761600
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.2700 血氧飽和測定儀;; E.2300 心臟監視器(包含心動數計和心率警示器)
Import Information
import
Dates and status
Registration Date
Sep 02, 2015
Expiry Date
Sep 02, 2025
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About this record

Access comprehensive regulatory information for "Nippon Opto" bedside monitor in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number ffe72fc6ee6c09392912cccb5d4c2963 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, 1 companies making similar products including Nihon Kohden Tomioka Corporation Tomioka Production Center, and 1 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.

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