GUDIDData
gudid Primary ID: 4457

NomoLine-O LH Pediatric Nasal CO2 Cannula with O2 (UDI 4457)

Manufactured by MASIMO CORPORATION

Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for NomoLine-O LH Pediatric Nasal CO2 Cannula with O2 - Primary ID 4457

Device Regulatory Overview

The NomoLine-O LH Pediatric Nasal CO2 Cannula with O2 (Model/Catalog Number: 4457) 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
4457
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
}
                            

Unlock Compliance Data & Serialization Specs

Access raw JSON payloads, UDI-DI packaging hierarchies, and Notified Body IDs.

Get API Token Access ($49/mo)

Frequently Asked Questions

Who is the primary manufacturer of NomoLine-O LH Pediatric Nasal CO2 Cannula with O2?

The registered manufacturer of record for NomoLine-O LH Pediatric Nasal CO2 Cannula with O2 is MASIMO CORPORATION.

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

The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 4457.

What classification code is assigned to this device?

This device is registered under product classification code CCK.

Programmatic Export

Export this master device record as standardized JSON or CSV for compliance audits.

JSON API Endpoint