eudamed_udi
Primary ID: 09330453306093
GUEDEL AIRWAY (UDI 09330453306093)
Manufactured by Fairmont Medical Products Pty Ltd
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for GUEDEL AIRWAY - Primary ID 09330453306093
Device Regulatory Overview
The GUEDEL AIRWAY (Model/Catalog Number: DGA9204NS) is a medical device manufactured by Fairmont Medical Products Pty Ltd. This product is indexed under FDA Product Code / Category Classification R010102 within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- DGA9204NS
- Product Code / EMDN
- R010102
- Device Name
- GUEDEL AIRWAY
- Database Sync Date
- 2026-08-09 16:28:53
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 GUEDEL AIRWAY?
The registered manufacturer of record for GUEDEL AIRWAY is Fairmont Medical Products Pty Ltd.
What is the Primary UDI-DI identifier for GUEDEL AIRWAY?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 09330453306093.
What classification code is assigned to this device?
This device is registered under product classification code R010102.
Similar Classification Devices (R010102)
Other Devices by Fairmont Medical Products Pty Ltd
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