Pure Global

“Nipro” Surefuser+ - Taiwan Registration 03f53c0d24840350d4a21e33e5bd1349

Access comprehensive regulatory information for “Nipro” Surefuser+ in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 03f53c0d24840350d4a21e33e5bd1349 and manufactured by Nipro Corporation Odate Factory. The authorized representative in Taiwan is HUA CHIANG 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
03f53c0d24840350d4a21e33e5bd1349
Registration Details
Taiwan FDA Registration: 03f53c0d24840350d4a21e33e5bd1349
Pure Global
DJ Fang

DJ Fang

MedTech Regulatory Expert

Need help with 30+ markets registration?

Pricing

Device Details

“Nipro” Surefuser+
TW: “尼普洛”微量輸液器
Risk Class 2
MD

Registration Details

03f53c0d24840350d4a21e33e5bd1349

Ministry of Health Medical Device Import No. 026107

DHA05602610700

Company Information

Product Details

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

J General hospital and personal use equipment

J5440 Intravascular infusion sleeve

Imported from abroad

Dates and Status

Apr 17, 2014

Apr 17, 2024