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"Medelai" intravenous indwelling needle - Taiwan Registration c6effab451af66b2d0db0e835a54ca6f

Access comprehensive regulatory information for "Medelai" intravenous indwelling needle in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number c6effab451af66b2d0db0e835a54ca6f and manufactured by Yangzhou Medline Industry Co., Ltd.. The authorized representative in Taiwan is EAFAN ENTERPRISE 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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c6effab451af66b2d0db0e835a54ca6f
Registration Details
Taiwan FDA Registration: c6effab451af66b2d0db0e835a54ca6f
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Device Details

"Medelai" intravenous indwelling needle
TW: โ€œ็พŽๅพท่Šโ€้œ่„ˆ็•™็ฝฎ้‡
Risk Class 2

Registration Details

c6effab451af66b2d0db0e835a54ca6f

DHA09200105401

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

Jul 31, 2019

Jul 31, 2024