eudamed_udi
Primary ID: 00606959024113
DreamStation Humidifier GER (UDI 00606959024113)
Manufactured by Respironics Inc.
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for DreamStation Humidifier GER - Primary ID 00606959024113
Device Regulatory Overview
The DreamStation Humidifier GER (Model/Catalog Number: DEXH) 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
- DEXH
- Product Code / EMDN
- R060201
- Device Name
- DreamStation Humidifier GER
- Database Sync Date
- 2026-08-09 17:08:46
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 DreamStation Humidifier GER?
The registered manufacturer of record for DreamStation Humidifier GER is Respironics Inc..
What is the Primary UDI-DI identifier for DreamStation Humidifier GER?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 00606959024113.
What classification code is assigned to this device?
This device is registered under product classification code R060201.
Similar Classification Devices (R060201)
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