GUDIDData
eudamed_udi Primary ID: 07045432082500

Laerdal Disposable PEEP Valve Assembly (UDI 07045432082500)

Manufactured by Laerdal Medical AS

Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for Laerdal Disposable PEEP Valve Assembly - Primary ID 07045432082500

Device Regulatory Overview

The Laerdal Disposable PEEP Valve Assembly (Model/Catalog Number: 845140) is a medical device manufactured by Laerdal Medical AS. This product is indexed under FDA Product Code / Category Classification R030280 within international Unique Device Identification (UDI) compliance databases.

Technical Specifications

Model Number
845140
Product Code / EMDN
R030280
Device Name
The BAG II Disposable Resuscitator
Database Sync Date
2026-08-09 17:17:49

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 Laerdal Disposable PEEP Valve Assembly?

The registered manufacturer of record for Laerdal Disposable PEEP Valve Assembly is Laerdal Medical AS.

What is the Primary UDI-DI identifier for Laerdal Disposable PEEP Valve Assembly?

The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 07045432082500.

What classification code is assigned to this device?

This device is registered under product classification code R030280.

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