gudid Primary ID: 2K8030

AirLife (UDI 2K8030)

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: 2K8030) is a medical device manufactured by AIRLIFE. This product is indexed under FDA Product Code / Category Classification BZR within international Unique Device Identification (UDI) compliance databases.

Technical Specifications

Model Number: 2K8030
Product Code / EMDN: BZR
Device Name: 3 Liter Neoprene Flow-Inflating Bag with Pre-Attached 7 (2.1 m) Oxygen Tubing and 7 (2.1 m) Manometer Tubing, Nonconductive
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 2K8030.

What classification code is assigned to this device?

This device is registered under product classification code BZR.

Similar Classification Devices (BZR)

Other Devices by AIRLIFE

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