enFlow (UDI 980121EU)

Manufactured by AIRLIFE

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

Scannable UDI-DI Representation

Device Regulatory Overview

The enFlow (Model/Catalog Number: 980121EU) is a medical device manufactured by AIRLIFE. This product is indexed under FDA Product Code / Category Classification LGZ within international Unique Device Identification (UDI) compliance databases.

Technical Specifications

Model Number: 980121EU
Product Code / EMDN: LGZ
Device Name: Controller Model 121
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 enFlow?

The registered manufacturer of record for enFlow is AIRLIFE.

What is the Primary UDI-DI identifier for enFlow?

The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 980121EU.

What classification code is assigned to this device?

This device is registered under product classification code LGZ.

Similar Classification Devices (LGZ)

Other Devices by AIRLIFE

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