gudid Primary ID: 5504BD

AirLife (UDI 5504BD)

Manufactured by AIRLIFE

Data verified against official FDA/EUDAMED records on August 9, 2026

Scannable UDI-DI Representation

Device Regulatory Overview

The AirLife (Model/Catalog Number: 5504BD) is a medical device manufactured by AIRLIFE. This product is indexed under FDA Product Code / Category Classification BZD within international Unique Device Identification (UDI) compliance databases.

Technical Specifications

Model Number: 5504BD
Product Code / EMDN: BZD
Device Name: AirLife Baby safe flow-inflating resuscitation device-1/2 Liter Bag
Database Sync Date: 2026-08-09 09:16:32

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 AirLife?

The registered manufacturer of record for AirLife is AIRLIFE.

What is the Primary UDI-DI identifier for AirLife?

The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 5504BD.

What classification code is assigned to this device?

This device is registered under product classification code BZD.

Similar Classification Devices (BZD)

Other Devices by AIRLIFE

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