Philips NightBalance, Refurbishment Kit, UK (UDI 00606959419940)
Manufactured by Respironics Inc.
Device Regulatory Overview
The Philips NightBalance, Refurbishment Kit, UK (Model/Catalog Number: RPL2EU01UK) 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
- RPL2EU01UK
- Product Code / EMDN
- Z12062402
- Device Name
- NightBalance
- Database Sync Date
- 2026-08-09 16:50:08
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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Get API Token Access ($49/mo)Frequently Asked Questions
Who is the primary manufacturer of Philips NightBalance, Refurbishment Kit, UK?
The registered manufacturer of record for Philips NightBalance, Refurbishment Kit, UK is Respironics Inc..
What is the Primary UDI-DI identifier for Philips NightBalance, Refurbishment Kit, UK?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 00606959419940.
What classification code is assigned to this device?
This device is registered under product classification code Z12062402.
Similar Classification Devices (Z12062402)
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