GUDIDData
eudamed_udi Primary ID: 06945429021356

High Flow Heated Respiratory Humidifier (UDI 06945429021356)

Manufactured by Shenzhen Comen Medical Instruments Co.,LTD.

Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for High Flow Heated Respiratory Humidifier - Primary ID 06945429021356

Device Regulatory Overview

The High Flow Heated Respiratory Humidifier (Model/Catalog Number: NF2) is a medical device manufactured by Shenzhen Comen Medical Instruments Co.,LTD.. This product is indexed under FDA Product Code / Category Classification R060201 within international Unique Device Identification (UDI) compliance databases.

Technical Specifications

Model Number
NF2
Product Code / EMDN
R060201
Device Name
High Flow Heated Respiratory Humidifier
Database Sync Date
2026-08-09 17:49:21

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 High Flow Heated Respiratory Humidifier?

The registered manufacturer of record for High Flow Heated Respiratory Humidifier is Shenzhen Comen Medical Instruments Co.,LTD..

What is the Primary UDI-DI identifier for High Flow Heated Respiratory Humidifier?

The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 06945429021356.

What classification code is assigned to this device?

This device is registered under product classification code R060201.

Programmatic Export

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

JSON API Endpoint