GUDIDData
eudamed_udi Primary ID: 06972091922063

BM Endotracheal Tube Introducers (bougie) (UDI 06972091922063)

Manufactured by Bonree Medical Co., Ltd.

Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for BM Endotracheal Tube Introducers (bougie) - Primary ID 06972091922063

Device Regulatory Overview

The BM Endotracheal Tube Introducers (bougie) (Model/Catalog Number: 20406002) is a medical device manufactured by Bonree Medical Co., Ltd.. This product is indexed under FDA Product Code / Category Classification R018004 within international Unique Device Identification (UDI) compliance databases.

Technical Specifications

Model Number
20406002
Product Code / EMDN
R018004
Device Name
Endotracheal Tube Introducers (bougie)
Database Sync Date
2026-08-09 16:30:03

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 BM Endotracheal Tube Introducers (bougie)?

The registered manufacturer of record for BM Endotracheal Tube Introducers (bougie) is Bonree Medical Co., Ltd..

What is the Primary UDI-DI identifier for BM Endotracheal Tube Introducers (bougie)?

The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 06972091922063.

What classification code is assigned to this device?

This device is registered under product classification code R018004.

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