Taiwan FDA registration deb88d6ac8f801d08131b050969f09ea

"Nippon Opto" bedside physiological monitor

TW: “日本光電”床邊生理監視器
Taiwan flagTaiwan·Risk Class 2·Nihon Kohden Tomioka Corporation Tomioka Production Center;; NIHON KOHDEN CORPORATION·Registered Apr 03, 2019 – Apr 03, 2029Active
Registration details
Analysis ID
deb88d6ac8f801d08131b050969f09ea
Customs Code
DHA05603255309
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.2300 Cardiac monitor (including cardiac data and heart rate monitor)
Import Information
import
Dates and status
Registration Date
Apr 03, 2019
Expiry Date
Apr 03, 2029
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About this record

Access comprehensive regulatory information for "Nippon Opto" bedside physiological monitor in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number deb88d6ac8f801d08131b050969f09ea 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, 2 companies making similar products including Nihon Kohden Tomioka Corporation Tomioka Production Center;; NIHON KOHDEN CORPORATION, Nihon Kohden Malaysia Sdn. Bhd.;; Jabil Circuit Sdn. Bhd., and 3 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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