gudid
Primary ID: 3809
NomoLine Adult Nasal/Oral CO2 Cannula with Luer (UDI 3809)
Manufactured by MASIMO CORPORATION
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for NomoLine Adult Nasal/Oral CO2 Cannula with Luer - Primary ID 3809
Device Regulatory Overview
The NomoLine Adult Nasal/Oral CO2 Cannula with Luer (Model/Catalog Number: 3809) is a medical device manufactured by MASIMO CORPORATION. This product is indexed under FDA Product Code / Category Classification CCK within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- 3809
- Product Code / EMDN
- CCK
- Device Name
- Database Sync Date
- 2026-08-09 09:21:51
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 NomoLine Adult Nasal/Oral CO2 Cannula with Luer?
The registered manufacturer of record for NomoLine Adult Nasal/Oral CO2 Cannula with Luer is MASIMO CORPORATION.
What is the Primary UDI-DI identifier for NomoLine Adult Nasal/Oral CO2 Cannula with Luer?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 3809.
What classification code is assigned to this device?
This device is registered under product classification code CCK.
Similar Classification Devices (CCK)
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