"Arno" percutaneous guide sheath group
Taiwan·Risk Class 2·ARROW INTERNATIONAL INC.·Registered Nov 02, 2010 – Nov 02, 2020Cancelled- Analysis ID
- d08c7fc5edf538348cc48c8d9bfd8202
- Customs Code
- DHA00602162800
- Manufacturer
- ARROW INTERNATIONAL INC.
- Manufacturer Country
- United States
- 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
- import
- Registration Date
- Nov 02, 2010
- Expiry Date
- Nov 02, 2020
- Cancellation Date
- Jun 07, 2022
- Status
- Logged out
- Reason
- 許可證已逾有效期
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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 d08c7fc5edf538348cc48c8d9bfd8202 and manufactured by ARROW INTERNATIONAL INC.. 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 INC., Arrow International, Inc. (Subsidiary of Teleflex Inc.);; Arrow International Cr, a.s., 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.