GUDIDData
gudid Primary ID: 3810

NomoLine Pediatric Nasal/Oral CO2 Cannula with Luer (UDI 3810)

Manufactured by MASIMO CORPORATION

Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for NomoLine Pediatric Nasal/Oral CO2 Cannula with Luer - Primary ID 3810

Device Regulatory Overview

The NomoLine Pediatric Nasal/Oral CO2 Cannula with Luer (Model/Catalog Number: 3810) 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
3810
Product Code / EMDN
CCK
Device Name
Database Sync Date
2026-08-09 09:21:51

Full Regulatory Attributes

🔒 Token Gated
{
    "review_panel": "AN",
    "gudid_di_status": "Published",
    "sterilization_methods": ["EO", "Gamma"],
    "rx_only": true
}
                            

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Frequently Asked Questions

Who is the primary manufacturer of NomoLine Pediatric Nasal/Oral CO2 Cannula with Luer?

The registered manufacturer of record for NomoLine Pediatric Nasal/Oral CO2 Cannula with Luer is MASIMO CORPORATION.

What is the Primary UDI-DI identifier for NomoLine Pediatric Nasal/Oral CO2 Cannula with Luer?

The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 3810.

What classification code is assigned to this device?

This device is registered under product classification code CCK.

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