gudid
Primary ID: IPN033988
ARROW (UDI IPN033988)
Manufactured by TELEFLEX INCORPORATED
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for ARROW - Primary ID IPN033988
Device Regulatory Overview
The ARROW (Model/Catalog Number: IPN033988) is a medical device manufactured by TELEFLEX INCORPORATED. This product is indexed under FDA Product Code / Category Classification MPB within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- IPN033988
- Product Code / EMDN
- MPB
- Device Name
- Two-Lumen Hemodialysis Catheterization Kit with Blue FlexTip(R) ARROWg+ard Blue(R) Catheter for High Volume Infusions
- Database Sync Date
- 2026-08-09 09:16:56
Full Regulatory Attributes
🔒 Token Gated
{
"review_panel": "AN",
"gudid_di_status": "Published",
"sterilization_methods": ["EO", "Gamma"],
"rx_only": true
}
Unlock Compliance Data & Serialization Specs
Access raw JSON payloads, UDI-DI packaging hierarchies, and Notified Body IDs.
Get API Token Access ($49/mo)Frequently Asked Questions
Who is the primary manufacturer of ARROW?
The registered manufacturer of record for ARROW is TELEFLEX INCORPORATED.
What is the Primary UDI-DI identifier for ARROW?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is IPN033988.
What classification code is assigned to this device?
This device is registered under product classification code MPB.
Similar Classification Devices (MPB)
Other Devices by TELEFLEX INCORPORATED
Programmatic Export
Export this master device record as standardized JSON or CSV for compliance audits.
JSON API Endpoint