gudid Primary ID: RP-1000

Nasal Interface, 3Pk (UDI RP-1000)

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

Scannable UDI-DI Representation

Device Regulatory Overview

The Nasal Interface, 3Pk (Model/Catalog Number: RP-1000) 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: RP-1000
Product Code / EMDN: ONZ
Device Name: Nasal Interface 3Pk, RP-1000
Database Sync Date: 2026-08-09 09:31:22

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 Nasal Interface, 3Pk?

The registered manufacturer of record for Nasal Interface, 3Pk is Inogen, Inc..

What is the Primary UDI-DI identifier for Nasal Interface, 3Pk?

The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is RP-1000.

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.

Programmatic Export

Export this master device record as standardized JSON or CSV for compliance audits.

JSON API Endpoint