gudid
Primary ID: 3822
NomoLine LH Adult Nasal/Oral CO2 Cannula (UDI 3822)
Manufactured by MASIMO CORPORATION
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for NomoLine LH Adult Nasal/Oral CO2 Cannula - Primary ID 3822
Device Regulatory Overview
The NomoLine LH Adult Nasal/Oral CO2 Cannula (Model/Catalog Number: 3822) 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
- 3822
- 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 LH Adult Nasal/Oral CO2 Cannula?
The registered manufacturer of record for NomoLine LH Adult Nasal/Oral CO2 Cannula is MASIMO CORPORATION.
What is the Primary UDI-DI identifier for NomoLine LH Adult Nasal/Oral CO2 Cannula?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 3822.
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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