GUDIDData
gudid Primary ID: 3808

NomoLine Pediatric Nasal CO2 Cannula with O2 and Luer (UDI 3808)

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 CO2 Cannula with O2 and Luer - Primary ID 3808

Device Regulatory Overview

The NomoLine Pediatric Nasal CO2 Cannula with O2 and Luer (Model/Catalog Number: 3808) 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
3808
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 CO2 Cannula with O2 and Luer?

The registered manufacturer of record for NomoLine Pediatric Nasal CO2 Cannula with O2 and Luer is MASIMO CORPORATION.

What is the Primary UDI-DI identifier for NomoLine Pediatric Nasal CO2 Cannula with O2 and Luer?

The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 3808.

What classification code is assigned to this device?

This device is registered under product classification code CCK.

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