Taiwan FDA registration 517f76167d0a09b7726c7e9bcd30883c
“Teleflex Arrow” Balloon Wedge Pressure Catheters
TW: “泰利福亞諾”肺動脈氣壓導管
Taiwan·Risk Class 2·MD·Arrow International, LLC (Subsidiary of Teleflex, Incorporated)·Registered May 31, 2018 – May 31, 2023ExpiredRegistration details
- Analysis ID
- 517f76167d0a09b7726c7e9bcd30883c
- License Form
- Ministry of Health Medical Device Import No. 030911
- Customs Code
- DHA05603091102
Company information
- Manufacturer Country
- United States
- 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 devices
- Product Type (Level 2)
- E1240 flow guide duct
- Import Information
- Imported from abroad
Dates and status
- Registration Date
- May 31, 2018
- Expiry Date
- May 31, 2023
About this record
Access comprehensive regulatory information for “Teleflex Arrow” Balloon Wedge Pressure Catheters in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 517f76167d0a09b7726c7e9bcd30883c and manufactured by Arrow International, LLC (Subsidiary of Teleflex, Incorporated). The authorized representative in Taiwan is TELEFLEX MEDICAL TAIWAN LTD..
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