eudamed_udi
Primary ID: 00619498281176
Lumis 150 VPAP ST EUR3 (UDI 00619498281176)
Manufactured by ResMed PTY LTD
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for Lumis 150 VPAP ST EUR3 - Primary ID 00619498281176
Device Regulatory Overview
The Lumis 150 VPAP ST EUR3 (Model/Catalog Number: 28117) is a medical device manufactured by ResMed PTY LTD. This product is indexed under FDA Product Code / Category Classification Z1203010504 within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- 28117
- Product Code / EMDN
- Z1203010504
- Device Name
- Lumis 100 VPAP S , Lumis 100 VPAP ST , Lumis 150 VPAP ST
- Database Sync Date
- 2026-08-09 16:29:36
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 Lumis 150 VPAP ST EUR3?
The registered manufacturer of record for Lumis 150 VPAP ST EUR3 is ResMed PTY LTD.
What is the Primary UDI-DI identifier for Lumis 150 VPAP ST EUR3?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 00619498281176.
What classification code is assigned to this device?
This device is registered under product classification code Z1203010504.
Similar Classification Devices (Z1203010504)
Other Devices by ResMed PTY LTD
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