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“Terumo” Neolus Needle - Taiwan Registration cc71fcae8868476261cfb0aa9adf6fd8

Access comprehensive regulatory information for “Terumo” Neolus Needle in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number cc71fcae8868476261cfb0aa9adf6fd8 and manufactured by TERUMO EUROPE N.V.. The authorized representative in Taiwan is TERUMO TAIWAN 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.

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cc71fcae8868476261cfb0aa9adf6fd8
Registration Details
Taiwan FDA Registration: cc71fcae8868476261cfb0aa9adf6fd8
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Device Details

“Terumo” Neolus Needle
TW: “泰爾茂” 尼歐拉斯注射針
Risk Class 2
MD

Registration Details

cc71fcae8868476261cfb0aa9adf6fd8

Ministry of Health Medical Device Import No. 034523

DHA05603452300

Company Information

Belgium

Product Details

Details are as detailed as approved Chinese instructions

J General hospital and personal use equipment

J5570 Subcutaneous single-lumen needle

Imported from abroad

Dates and Status

May 12, 2021

May 12, 2026