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"Luci" ureter - Taiwan Registration 54c30bde72c212cac2c36074eee7be05

Access comprehensive regulatory information for "Luci" ureter in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 54c30bde72c212cac2c36074eee7be05 and manufactured by TELEFLEX MEDICAL;; ARROW INTERNATIONAL CR A.S.. The authorized representative in Taiwan is TELEFLEX MEDICAL TAIWAN LTD..

This page provides complete technical specifications, regulatory compliance details, 1 companies making similar products including Teleflex Medical; Arrow International CR, a.s. Branch in ลฝฤรกr nad Sรกzavou, 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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54c30bde72c212cac2c36074eee7be05
Registration Details
Taiwan FDA Registration: 54c30bde72c212cac2c36074eee7be05
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Device Details

"Luci" ureter
TW: โ€œ่ทฏๅธŒโ€่ผธๅฐฟๅฐŽ็ฎก
Risk Class 2

Registration Details

54c30bde72c212cac2c36074eee7be05

DHA05603137200

Company Information

Iran, Islamic Republic of;;Czechia

Product Details

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

H Gastroenterology and urology

H.5130 ๆณŒๅฐฟๅฐŽ็ฎกๅŠๅ…ถ้™„ไปถ

Input;; Contract manufacturing

Dates and Status

Jul 27, 2018

Jul 27, 2028

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