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"Termao" Yagani needle - Taiwan Registration 21f4a082ced95bee5cfceb7032b99500

Access comprehensive regulatory information for "Termao" Yagani needle in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 21f4a082ced95bee5cfceb7032b99500 and manufactured by Zhejiang Kindly Medical Devices Co., Ltd.. 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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21f4a082ced95bee5cfceb7032b99500
Registration Details
Taiwan FDA Registration: 21f4a082ced95bee5cfceb7032b99500
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Device Details

"Termao" Yagani needle
TW: โ€œๆณฐ็ˆพ่Œ‚โ€ไบžๅŠ ๅฐผ้‡้ ญ
Risk Class 2

Registration Details

21f4a082ced95bee5cfceb7032b99500

DHA04200053503

Company Information

Product Details

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

J General hospital and personal use equipment

J.5570 Subcutaneous single-chamber needle

Chinese goods;; input

Dates and Status

May 25, 2013

May 25, 2028