Taiwan FDA registration 0626700459845761fe1aa4df974c1591

"Luci" ureteral stent

TW: “路希”輸尿管支架

Taiwan·Risk Class 2·Teleflex Medical; Arrow International CR, a.s. Branch in Žďár nad Sázavou·Registered Jan 23, 2019 – Jan 23, 2029Active

Registration details

Analysis ID: 0626700459845761fe1aa4df974c1591
Customs Code: DHA05603222100

Company information

Manufacturer: Teleflex Medical; Arrow International CR, a.s. Branch in Žďár nad Sázavou
Manufacturer Country: Ireland;;Czechia
Authorized Representative: TELEFLEX MEDICAL TAIWAN LTD.

Product details

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.4620 Urinary Catheter Stent
Import Information: Input;; Contract manufacturing

Dates and status

Registration Date: Jan 23, 2019
Expiry Date: Jan 23, 2029

About this record

Access comprehensive regulatory information for "Luci" ureteral stent in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 0626700459845761fe1aa4df974c1591 and manufactured by Teleflex Medical; Arrow International CR, a.s. Branch in Žďár nad Sázavou. The authorized representative in Taiwan is TELEFLEX MEDICAL TAIWAN LTD..

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