Arrowg+ard Blue(R) Three-Lumen CVC (UDI 10801902165609)
Manufactured by Arrow International LLC (Subsidiary of Teleflex Incorporated)
Device Regulatory Overview
The Arrowg+ard Blue(R) Three-Lumen CVC (Model/Catalog Number: DE-24703S-AGK) is a medical device manufactured by Arrow International LLC (Subsidiary of Teleflex Incorporated). This product is indexed under FDA Product Code / Category Classification C01020203 within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- DE-24703S-AGK
- Product Code / EMDN
- C01020203
- Device Name
- AGB CVC Procedure Pack
- Database Sync Date
- 2026-08-09 16:28:47
Full Regulatory Attributes
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{
"review_panel": "AN",
"gudid_di_status": "Published",
"sterilization_methods": ["EO", "Gamma"],
"rx_only": true
}
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Get API Token Access ($49/mo)Frequently Asked Questions
Who is the primary manufacturer of Arrowg+ard Blue(R) Three-Lumen CVC?
The registered manufacturer of record for Arrowg+ard Blue(R) Three-Lumen CVC is Arrow International LLC (Subsidiary of Teleflex Incorporated).
What is the Primary UDI-DI identifier for Arrowg+ard Blue(R) Three-Lumen CVC?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 10801902165609.
What classification code is assigned to this device?
This device is registered under product classification code C01020203.
Similar Classification Devices (C01020203)
Other Devices by Arrow International LLC (Subsidiary of Teleflex Incorporated)
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