gudid Primary ID: 10-09815-XX-01

TAV Nasal Interface (UDI 10-09815-XX-01)

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

Scannable UDI-DI Representation

Device Regulatory Overview

The TAV Nasal Interface (Model/Catalog Number: 10-09815-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: 10-09815-XX-01
Product Code / EMDN: ONZ
Device Name: TAV Nasal Interface (10-09815-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 Nasal Interface?

The registered manufacturer of record for TAV Nasal Interface is Inogen, Inc..

What is the Primary UDI-DI identifier for TAV Nasal Interface?

The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 10-09815-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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