"Telifiano" percutaneous guide sheath set
Taiwan·Risk Class 2·Arrow International C.R. a.s.;; Arrow International LLC(Subsidiary of Teleflex Incorporated)·Registered Mar 20, 2018 – Mar 20, 2023Expired- Analysis ID
- ca737a9a755bda08b9d81ab5142a192a
- Customs Code
- DHA05603077708
- 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.1340 Catheter Introducers
- Import Information
- Contract manufacturing;; input
- Registration Date
- Mar 20, 2018
- Expiry Date
- Mar 20, 2023
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Access comprehensive regulatory information for "Telifiano" percutaneous guide sheath set in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number ca737a9a755bda08b9d81ab5142a192a 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, 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.