"Telifano" multi-lumen central venous catheter
Taiwan·Risk Class 2·ARROW INTERNATIONAL INC.·Registered May 02, 2018 – May 02, 2023Expired- Analysis ID
- 65979ed836368951f548c77646bc23f4
- Customs Code
- DHA05603088906
- Manufacturer
- ARROW INTERNATIONAL INC.
- Manufacturer Country
- United States
- 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 02, 2018
- Expiry Date
- May 02, 2023
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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 65979ed836368951f548c77646bc23f4 and manufactured by ARROW INTERNATIONAL INC.. 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 C.R. a.s.;; Arrow International LLC(Subsidiary of Teleflex Incorporated), 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.