Taiwan FDA registration d3d4fc7e9607eb76c204872880ff12b1
“Teleflex Arrow” ARROWgard Catheters
TW: “泰利福亞諾”抗感染中央靜脈導管套組
Taiwan·Risk Class 2·MD·ARROW INTERNATIONAL INC.·Registered Apr 16, 2018 – Apr 16, 2023ExpiredRegistration details
- Analysis ID
- d3d4fc7e9607eb76c204872880ff12b1
- License Form
- Ministry of Health Medical Device Import No. 030806
- Customs Code
- DHA05603080602
Company information
- Manufacturer
- ARROW INTERNATIONAL INC.
- 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)
- J General hospital and personal use equipment
- Product Type (Level 2)
- J5200 Intravascular catheter
- Import Information
- Imported from abroad
Dates and status
- Registration Date
- Apr 16, 2018
- Expiry Date
- Apr 16, 2023
About this record
Access comprehensive regulatory information for “Teleflex Arrow” ARROWgard Catheters in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number d3d4fc7e9607eb76c204872880ff12b1 and manufactured by ARROW INTERNATIONAL INC.. The authorized representative in Taiwan is TELEFLEX MEDICAL TAIWAN LTD..
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