GUDIDData
gudid Primary ID: 4449

NomoLine-O HH Adult/Pediatric Airway Adapter Set (UDI 4449)

Manufactured by MASIMO CORPORATION

Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for NomoLine-O HH Adult/Pediatric Airway Adapter Set - Primary ID 4449

Device Regulatory Overview

The NomoLine-O HH Adult/Pediatric Airway Adapter Set (Model/Catalog Number: 4449) 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
4449
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 HH Adult/Pediatric Airway Adapter Set?

The registered manufacturer of record for NomoLine-O HH Adult/Pediatric Airway Adapter Set is MASIMO CORPORATION.

What is the Primary UDI-DI identifier for NomoLine-O HH Adult/Pediatric Airway Adapter Set?

The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 4449.

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