GUDIDData
gudid Primary ID: 845151

The BAG II Resuscitator Adult mask #5 w/inf.port (UDI 845151)

Manufactured by Laerdal Medical AS

Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for The BAG II Resuscitator Adult mask #5 w/inf.port - Primary ID 845151

Device Regulatory Overview

The The BAG II Resuscitator Adult mask #5 w/inf.port (Model/Catalog Number: 845151) is a medical device manufactured by Laerdal Medical AS. This product is indexed under FDA Product Code / Category Classification BTM within international Unique Device Identification (UDI) compliance databases.

Technical Specifications

Model Number
845151
Product Code / EMDN
BTM
Device Name
The BAG II are manual resuscitators incorporating a bag and valve, intended to provide emergency ventilation or ventilation during patient transport. The infant model is intended for patients weighing between 5 to 12 kgs, the child model is intended for patients weighing between 10 to 30 kgs, and the adult model is intended for patients weighing more than 30 kgs approximate weight. The SIMPLIFY COMPACT RESUSCITATOR provided in reusable models and in the disposable models.
Database Sync Date
2026-08-09 09:18:19

Full Regulatory Attributes

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{
    "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 The BAG II Resuscitator Adult mask #5 w/inf.port?

The registered manufacturer of record for The BAG II Resuscitator Adult mask #5 w/inf.port is Laerdal Medical AS.

What is the Primary UDI-DI identifier for The BAG II Resuscitator Adult mask #5 w/inf.port?

The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 845151.

What classification code is assigned to this device?

This device is registered under product classification code BTM.

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