"Luci" ureter
Taiwan·Risk Class 2·TELEFLEX MEDICAL;; ARROW INTERNATIONAL CR A.S.·Registered Jul 27, 2018 – Jul 27, 2028Active- Analysis ID
- 54c30bde72c212cac2c36074eee7be05
- Customs Code
- DHA05603137200
- Manufacturer
- TELEFLEX MEDICAL;; ARROW INTERNATIONAL CR A.S.
- Manufacturer Country
- Iran, Islamic Republic of;;Czechia
- Authorized Representative
- TELEFLEX MEDICAL TAIWAN LTD.
- Intended Use
- For details, it is Chinese approved copy of the imitation order
- Product Type (Level 1)
- H Gastroenterology and urology
- Product Type (Level 2)
- H.5130 泌尿導管及其附件
- Import Information
- Input;; Contract manufacturing
- Registration Date
- Jul 27, 2018
- Expiry Date
- Jul 27, 2028
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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 Žďár nad Sázavou, 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.