eudamed_udi Primary ID: 00606959419629

Philips NightBalance Mobile App, Android (UDI 00606959419629)

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

Scannable UDI-DI Representation

Device Regulatory Overview

The Philips NightBalance Mobile App, Android (Model/Catalog Number: 1142207) is a medical device manufactured by Respironics Inc.. This product is indexed under FDA Product Code / Category Classification Z12062402 within international Unique Device Identification (UDI) compliance databases.

Technical Specifications

Model Number: 1142207
Product Code / EMDN: Z12062402
Device Name: NightBalance
Database Sync Date: 2026-08-09 16:50:18

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 Philips NightBalance Mobile App, Android?

The registered manufacturer of record for Philips NightBalance Mobile App, Android is Respironics Inc..

What is the Primary UDI-DI identifier for Philips NightBalance Mobile App, Android?

The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 00606959419629.

What classification code is assigned to this device?

This device is registered under product classification code Z12062402.

Similar Classification Devices (Z12062402)

Other Devices by Respironics Inc.

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