eudamed_udi
Primary ID: 00619498627844
NV Quattro Air FFM MED - EUR (UDI 00619498627844)
Manufactured by ResMed PTY LTD
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for NV Quattro Air FFM MED - EUR - Primary ID 00619498627844
Device Regulatory Overview
The NV Quattro Air FFM MED - EUR (Model/Catalog Number: 62784) is a medical device manufactured by ResMed PTY LTD. This product is indexed under FDA Product Code / Category Classification R0301010202 within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- 62784
- Product Code / EMDN
- R0301010202
- Device Name
- Quattro Air NV
- Database Sync Date
- 2026-08-09 16:29:26
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 NV Quattro Air FFM MED - EUR?
The registered manufacturer of record for NV Quattro Air FFM MED - EUR is ResMed PTY LTD.
What is the Primary UDI-DI identifier for NV Quattro Air FFM MED - EUR?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 00619498627844.
What classification code is assigned to this device?
This device is registered under product classification code R0301010202.
Similar Classification Devices (R0301010202)
Other Devices by ResMed PTY LTD
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