Taiwan FDA registration f1823b6ffb7935ae1f3d4e6f5624d640
"Arno" ductus arteriosus sleeve
TW: “亞諾”動脈導管套組
Taiwan·Risk Class 2·Arrow International LLC (subsidiary of Teleflex Incorporated);; Arrow International Cr, a.s.·Registered Aug 26, 2020 – Aug 26, 2025ExpiredRegistration details
- Analysis ID
- f1823b6ffb7935ae1f3d4e6f5624d640
- Customs Code
- DHA05603390404
Company information
- Manufacturer
- Arrow International LLC (subsidiary of Teleflex Incorporated);; Arrow International Cr, a.s.
- Manufacturer Country
- United States;;Czechia
- Authorized Representative
- TELEFLEX MEDICAL TAIWAN LTD.
Product details
- 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
Dates and status
- Registration Date
- Aug 26, 2020
- Expiry Date
- Aug 26, 2025
About this record
Access comprehensive regulatory information for "Arno" ductus arteriosus sleeve in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number f1823b6ffb7935ae1f3d4e6f5624d640 and manufactured by Arrow International LLC (subsidiary of Teleflex Incorporated);; Arrow International Cr, a.s.. The authorized representative in Taiwan is TELEFLEX MEDICAL TAIWAN LTD..
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