gudid Primary ID: 10-09889-XX-01

TAV 7ft O2 Delivery Tubing (UDI 10-09889-XX-01)

Data verified against official FDA/EUDAMED records on August 9, 2026

Scannable UDI-DI Representation

Device Regulatory Overview

The TAV 7ft O2 Delivery Tubing (Model/Catalog Number: 10-09889-XX-01) is a medical device manufactured by Inogen, Inc.. This product is indexed under FDA Product Code / Category Classification ONZ within international Unique Device Identification (UDI) compliance databases.

Technical Specifications

Model Number: 10-09889-XX-01
Product Code / EMDN: ONZ
Device Name: TAV 7ft O2 Delivery Tubing, 10-09889-XX-01
Database Sync Date: 2026-08-09 09:31:22

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 TAV 7ft O2 Delivery Tubing?

The registered manufacturer of record for TAV 7ft O2 Delivery Tubing is Inogen, Inc..

What is the Primary UDI-DI identifier for TAV 7ft O2 Delivery Tubing?

The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 10-09889-XX-01.

What classification code is assigned to this device?

This device is registered under product classification code ONZ.

Similar Classification Devices (ONZ)

Other Devices by Inogen, Inc.

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