Taiwan FDA registration d198bdca3b80b00e619c338173beab10

"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 Feb 21, 2020 – Feb 21, 2030Active
Registration details
Analysis ID
d198bdca3b80b00e619c338173beab10
Customs Code
DHA05603324809
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
Feb 21, 2020
Expiry Date
Feb 21, 2030
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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 d198bdca3b80b00e619c338173beab10 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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