"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 ลฝฤรกr 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.
Device Details
Registration Details
54c30bde72c212cac2c36074eee7be05
DHA05603137200
Product Details
For details, it is Chinese approved copy of the imitation order
H Gastroenterology and urology
H.5130 ๆณๅฐฟๅฐ็ฎกๅๅ ถ้ไปถ
Input;; Contract manufacturing
Dates and Status
Jul 27, 2018
Jul 27, 2028

