"Telifano" anti-infective pressure injection type peripherally placed in 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 Oct 12, 2021 – Oct 12, 2026Active- Analysis ID
- d2fc21adf42ef10e87a163fb1e8440b5
- Customs Code
- DHA05603487107
- Manufacturer Country
- Mexico;;United States
- Authorized Representative
- TELEFLEX MEDICAL TAIWAN LTD.
- Intended Use
- Details are as detailed as approved Chinese instructions
- 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
- import
- Registration Date
- Oct 12, 2021
- Expiry Date
- Oct 12, 2026
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Access comprehensive regulatory information for "Telifano" anti-infective pressure injection type peripherally placed in 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 d2fc21adf42ef10e87a163fb1e8440b5 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, 1 companies making similar products including Arrow Internacional de Chihuahua S.A. de C.V.;; Arrow International LLC (subsidiary of Teleflex Incorporated), and 1 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.