"Arno" ductus arteriosus group
- Analysis ID
- c2c8184ed34de2853b5bd5000149d188
- Customs Code
- DHA00602161501
- Manufacturer Country
- Mexico;;United States
- Authorized Representative
- TELEFLEX MEDICAL TAIWAN LTD.
- Intended Use
- Details such as Chinese imitation slip approval of changes to this application: Label, instruction manual or packaging and indication changes: details such as the approved Chinese instruction manual (the original label, instruction manual or packaging approved on October 20, 111 shall be withdrawn and invalidated).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
- Oct 29, 2010
- Expiry Date
- Oct 29, 2025
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Access comprehensive regulatory information for "Arno" ductus arteriosus group in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number c2c8184ed34de2853b5bd5000149d188 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, 3 companies making similar products including ARROW INTERNATIONAL INC., Arrow Internacional de Chihuahua S.A. de C.V.;; Arrow International LLC (subsidiary of Teleflex Incorporated), and 3 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.