GUDIDData
eudamed_udi Primary ID: 00606959424609

DreamStation Auto CPAP with Humidifier, AU (UDI 00606959424609)

Manufactured by Respironics Inc.

Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for DreamStation Auto CPAP with Humidifier, AU - Primary ID 00606959424609

Device Regulatory Overview

The DreamStation Auto CPAP with Humidifier, AU (Model/Catalog Number: AUX500H15) is a medical device manufactured by Respironics Inc.. This product is indexed under FDA Product Code / Category Classification Z12030102 within international Unique Device Identification (UDI) compliance databases.

Technical Specifications

Model Number
AUX500H15
Product Code / EMDN
Z12030102
Device Name
DreamStation Auto CPAP with Humidifier, AU
Database Sync Date
2026-08-09 16:28:52

Full Regulatory Attributes

🔒 Token Gated
{
    "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 DreamStation Auto CPAP with Humidifier, AU?

The registered manufacturer of record for DreamStation Auto CPAP with Humidifier, AU is Respironics Inc..

What is the Primary UDI-DI identifier for DreamStation Auto CPAP with Humidifier, AU?

The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 00606959424609.

What classification code is assigned to this device?

This device is registered under product classification code Z12030102.

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