"Telifano" multi-lumen central venous catheter
Taiwan·Risk Class 2·Arrow International C.R. a.s.;; Arrow International LLC(Subsidiary of Teleflex Incorporated)·Registered May 01, 2018 – May 01, 2023Expired- Analysis ID
- 0e37968c71bf569a11b6aba324663f06
- Customs Code
- DHA05603088307
- 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)
- J General hospital and personal use equipment
- Product Type (Level 2)
- J.5200 Endovascular catheters
- Import Information
- Input;; Contract manufacturing
- Registration Date
- May 01, 2018
- Expiry Date
- May 01, 2023
Top companies providing products similar to ""Telifano" multi-lumen central venous catheter"
Recently registered similar products
Access comprehensive regulatory information for "Telifano" multi-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 0e37968c71bf569a11b6aba324663f06 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, 2 companies making similar products including Arrow Internacional de Chihuahua S.A. de C.V.;; Arrow International LLC (subsidiary of Teleflex Incorporated), ARROW INTERNATIONAL INC., and 2 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.