"Telifiano" Single lumen central venous catheter
- Analysis ID
- be53577d14a4d1b6f92e177c485a6986
- Customs Code
- DHA05603080401
- Manufacturer
- Arrow International C.R. a.s.;; Arrow International LLC(Subsidiary of Teleflex Incorporated)
- Manufacturer Country
- United States;;Czechia
- Authorized Representative
- TELEFLEX MEDICAL TAIWAN LTD.
- Intended Use
- For details, it is Chinese approved copy of the imitation order
- Product Type (Level 1)
- E Cardiovascular Medicine Science
- Product Type (Level 2)
- E.1200 診斷用血管內導管
- Import Information
- Input;; Contract manufacturing
- Registration Date
- Apr 16, 2018
- Expiry Date
- Apr 16, 2023
Access comprehensive regulatory information for "Telifiano" Single lumen central venous catheter in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number be53577d14a4d1b6f92e177c485a6986 and manufactured by Arrow International C.R. a.s.;; Arrow International LLC(Subsidiary of Teleflex Incorporated). The authorized representative in Taiwan is TELEFLEX MEDICAL TAIWAN 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.