GUDIDData
gudid Primary ID: IPN919672

ARROW (UDI IPN919672)

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 IPN919672

Device Regulatory Overview

The ARROW (Model/Catalog Number: IPN919672) is a medical device manufactured by TELEFLEX INCORPORATED. This product is indexed under FDA Product Code / Category Classification DYB within international Unique Device Identification (UDI) compliance databases.

Technical Specifications

Model Number
IPN919672
Product Code / EMDN
DYB
Device Name
Database Sync Date
2026-08-09 09:00:28

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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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 IPN919672.

What classification code is assigned to this device?

This device is registered under product classification code DYB.

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