gudid Primary ID: 1997-504

AirLife (UDI 1997-504)

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: 1997-504) is a medical device manufactured by AIRLIFE. This product is indexed under FDA Product Code / Category Classification BZE within international Unique Device Identification (UDI) compliance databases.

Technical Specifications

Model Number: 1997-504
Product Code / EMDN: BZE
Device Name: Isothermal Breathing Circuit Adult Inspiratory Line Heated
Database Sync Date: 2026-08-09 09:16:36

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 1997-504.

What classification code is assigned to this device?

This device is registered under product classification code BZE.

Similar Classification Devices (BZE)

Other Devices by AIRLIFE

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