eudamed_udi
Primary ID: 00619498646173
AIRFIT F40 SYS - M/SML EU1 (UDI 00619498646173)
Manufactured by ResMed PTY LTD
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for AIRFIT F40 SYS - M/SML EU1 - Primary ID 00619498646173
Device Regulatory Overview
The AIRFIT F40 SYS - M/SML EU1 (Model/Catalog Number: 64617) is a medical device manufactured by ResMed PTY LTD. This product is indexed under FDA Product Code / Category Classification R0301010201 within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- 64617
- Product Code / EMDN
- R0301010201
- Device Name
- AirFit F40
- Database Sync Date
- 2026-08-09 16:45:01
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 AIRFIT F40 SYS - M/SML EU1?
The registered manufacturer of record for AIRFIT F40 SYS - M/SML EU1 is ResMed PTY LTD.
What is the Primary UDI-DI identifier for AIRFIT F40 SYS - M/SML EU1?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 00619498646173.
What classification code is assigned to this device?
This device is registered under product classification code R0301010201.
Similar Classification Devices (R0301010201)
Other Devices by ResMed PTY LTD
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