gudid Primary ID: 9022B

AirLife (UDI 9022B)

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: 9022B) is a medical device manufactured by AIRLIFE. This product is indexed under FDA Product Code / Category Classification BYE within international Unique Device Identification (UDI) compliance databases.

Technical Specifications

Model Number: 9022B
Product Code / EMDN: BYE
Device Name: AirLife bi-directional flow guard PEEP valve
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 9022B.

What classification code is assigned to this device?

This device is registered under product classification code BYE.

Similar Classification Devices (BYE)

Other Devices by AIRLIFE

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