"Arno" percutaneous guide sheath group
Taiwan·Risk Class 2·Arrow International, Inc. (Subsidiary of Teleflex Inc.);; Arrow International Cr, a.s.·Registered Jul 02, 2014 – Jul 02, 2029Active- Analysis ID
- a34b4647c00dc7bede8b0a2c1573e4b1
- Customs Code
- DHA05602638400
- Manufacturer Country
- United States;;Czechia
- Authorized Representative
- TELEFLEX MEDICAL TAIWAN LTD.
- Intended Use
- Details as in the Chinese copy of the approved copy Application for change: change in efficacy, use or indications: detailed as the approved Chinese instruction manual (the original label, instruction manual or packaging approved on March 1, 111 will be withdrawn and invalidated).
- Product Type (Level 1)
- E Cardiovascular Medicine Science
- Product Type (Level 2)
- E.1340 Catheter Introducers
- Import Information
- import
- Registration Date
- Jul 02, 2014
- Expiry Date
- Jul 02, 2029
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Access comprehensive regulatory information for "Arno" percutaneous guide sheath group in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number a34b4647c00dc7bede8b0a2c1573e4b1 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 INTERNATIONAL INC., Arrow Internacional de Chihuahua S.A. de C.V.;; ARROW INTERNATIONAL INC., and 2 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.