"Telifano" anti-infective advanced peripheral placement into the central venous catheter group
Taiwan·Risk Class 2·Arrow Internacional de Chihuahua S.A. de C.V.;; Arrow International LLC (subsidiary of Teleflex Incorporated)·Registered Nov 09, 2019 – Nov 09, 2029Active- Analysis ID
- 65bcebe7a51a2b524b4f6f4ec7a24d12
- Customs Code
- DHA05603291708
- Manufacturer Country
- Mexico;;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.5970 Percutaneous long-term implantable endovascular catheters
- Import Information
- Contract manufacturing;; input
- Registration Date
- Nov 09, 2019
- Expiry Date
- Nov 09, 2029
Access comprehensive regulatory information for "Telifano" anti-infective advanced peripheral placement into the central venous catheter group in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 65bcebe7a51a2b524b4f6f4ec7a24d12 and manufactured by Arrow Internacional de Chihuahua S.A. de C.V.;; 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.