Pure Global

"Nippon Optoelectronics" defibrillator system - Taiwan Registration 6d5844a56c2f7836af9bcef84347bb1a

Access comprehensive regulatory information for "Nippon Optoelectronics" defibrillator system in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 3 medical device is registered under number 6d5844a56c2f7836af9bcef84347bb1a 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. 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.

Free Database
Powered by Pure Global AI
89,000+ Devices
6d5844a56c2f7836af9bcef84347bb1a
Registration Details
Taiwan FDA Registration: 6d5844a56c2f7836af9bcef84347bb1a
Pure Global
DJ Fang

DJ Fang

MedTech Regulatory Expert

Need help with 30+ markets registration?

Pricing

Device Details

"Nippon Optoelectronics" defibrillator system
TW: โ€œๆ—ฅๆœฌๅ…‰้›ปโ€ๅŽป้กซๅ™จ็ณป็ตฑ
Risk Class 3

Registration Details

6d5844a56c2f7836af9bcef84347bb1a

DHA05603396600

Product Details

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

E Cardiovascular Medicine Science

E.5310 ่‡ชๅ‹•้ซ”ๅค–ๅŽป้กซๅ™จ็ณป็ตฑ

import

Dates and Status

Sep 26, 2020

Sep 26, 2025