"Arno" single-lumen central venous catheter group
- Analysis ID
- c57fef6b9bc276b0798a5291a2fbfc8f
- Customs Code
- DHA05602692100
- Manufacturer Country
- United States;;Czechia
- Authorized Representative
- TELEFLEX MEDICAL TAIWAN LTD.
- Intended Use
- Details such as the validity of the Chinese imitation single approved version of the application is changed to: detailed as the approved Chinese instruction manual (the original approved label, instruction manual or packaging on January 16, 104 will be withdrawn and invalidated). The efficacy, use or indication is changed to: detailed as the approved Chinese instruction manual (the original label, instruction manual or packaging approved on January 16, 104 shall be withdrawn and invalidated).
- Product Type (Level 1)
- E Cardiovascular Medicine Science
- Product Type (Level 2)
- E.1200 診斷用血管內導管
- Import Information
- import
- Registration Date
- Dec 30, 2014
- Expiry Date
- Dec 30, 2029
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Access comprehensive regulatory information for "Arno" single-lumen 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 c57fef6b9bc276b0798a5291a2fbfc8f and manufactured by Arrow International CR, a.s.;; Arrow International, Inc.(Subsidiary of Teleflex Inc.). 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.