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"Youle" Yeke membrane pipeline group - Taiwan Registration 3b121acf2f34eea7ff331fdd19d8a16b

Access comprehensive regulatory information for "Youle" Yeke membrane pipeline group in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 3 medical device is registered under number 3b121acf2f34eea7ff331fdd19d8a16b and manufactured by EUROSETS S.r.l.. The authorized representative in Taiwan is EUDORA MEDICAL TECHNOLOGY 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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3b121acf2f34eea7ff331fdd19d8a16b
Registration Details
Taiwan FDA Registration: 3b121acf2f34eea7ff331fdd19d8a16b
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Device Details

"Youle" Yeke membrane pipeline group
TW: โ€œๅ„ชๆจ‚โ€ ่‘‰ๅ…‹่†œ็ฎก่ทฏ็ต„
Risk Class 3

Registration Details

3b121acf2f34eea7ff331fdd19d8a16b

DHA05603742907

Company Information

Italy

Product Details

Details are as detailed as approved Chinese instructions

E Cardiovascular Medicine Science

E.4350 ๅฟƒ่‚บ่ก€็ฎก็นž้“่ก“ๅ’Œๆฐงๅ™จ;; E.4360 ้žๆปพ็ญ’ๅผๅฟƒ่‚บ่ก€็ฎก็นž้“่ก“่ก€ๆถฒๅพช็’ฐๅนซๆตฆ

import

Dates and Status

Oct 11, 2024

Oct 11, 2029