"Arno" ductus arteriosus group
Taiwan·Risk Class 2·Arrow International, Inc. (Subsidiary of Teleflex Inc.);; Arrow International CR, a.s.·Registered Aug 18, 2014 – Aug 18, 2024Expired- Analysis ID
- 6b3238d92b50aa7997b883cc39fced3b
- Customs Code
- DHA05602643902
- 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.1250 Percutaneous catheters
- Import Information
- import
- Registration Date
- Aug 18, 2014
- Expiry Date
- Aug 18, 2024
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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 6b3238d92b50aa7997b883cc39fced3b and manufactured by Arrow International, Inc. (Subsidiary of Teleflex Inc.);; Arrow International CR, a.s.. The authorized representative in Taiwan is TELEFLEX MEDICAL TAIWAN LTD..
This page provides complete technical specifications, regulatory compliance details, 2 companies making similar products including Arrow Internacional de Chihuahua S.A. de C.V.;; Arrow International LLC (subsidiary of Teleflex Incorporated), ARROW INTERNATIONAL INC., 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.