eudamed_udi Primary ID: 00606959056831

A40 Pro/EFL, Sys One Heated Hum, Intl (UDI 00606959056831)

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

Scannable UDI-DI Representation

Device Regulatory Overview

The A40 Pro/EFL, Sys One Heated Hum, Intl (Model/Catalog Number: INX3H) is a medical device manufactured by Respironics Inc.. This product is indexed under FDA Product Code / Category Classification R060201 within international Unique Device Identification (UDI) compliance databases.

Technical Specifications

Model Number: INX3H
Product Code / EMDN: R060201
Device Name: A40 Pro/EFL, Sys One Heated Hum, Intl
Database Sync Date: 2026-08-09 16:44:49

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 A40 Pro/EFL, Sys One Heated Hum, Intl?

The registered manufacturer of record for A40 Pro/EFL, Sys One Heated Hum, Intl is Respironics Inc..

What is the Primary UDI-DI identifier for A40 Pro/EFL, Sys One Heated Hum, Intl?

The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 00606959056831.

What classification code is assigned to this device?

This device is registered under product classification code R060201.

Similar Classification Devices (R060201)

Other Devices by Respironics Inc.

Programmatic Export

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

JSON API Endpoint