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"Ruxi" IV lancet - Taiwan Registration 2dbedc6329c7ae8bd10162ac463fb4de

Access comprehensive regulatory information for "Ruxi" IV lancet in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 2dbedc6329c7ae8bd10162ac463fb4de 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, 1 companies making similar products including Yangzhou Medline Industry Co., Ltd., and 1 recent registrations in the same category. 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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2dbedc6329c7ae8bd10162ac463fb4de
Registration Details
Taiwan FDA Registration: 2dbedc6329c7ae8bd10162ac463fb4de
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Device Details

"Ruxi" IV lancet
TW: โ€œๅฆ‚็ฆงโ€ ้œ่„ˆๆŽก่ก€้‡
Risk Class 2

Registration Details

2dbedc6329c7ae8bd10162ac463fb4de

DHA09200107404

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

Input;; Chinese goods

Dates and Status

Oct 17, 2019

Oct 17, 2024

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