BROSELOW (UDI 7700WAW)

Manufactured by AIRLIFE

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

Scannable UDI-DI Representation

Device Regulatory Overview

The BROSELOW (Model/Catalog Number: 7700WAW) is a medical device manufactured by AIRLIFE. This product is indexed under FDA Product Code / Category Classification OKI within international Unique Device Identification (UDI) compliance databases.

Technical Specifications

Model Number: 7700WAW
Product Code / EMDN: OKI
Device Name: BROSELOW OXYGEN DELIVERY MODULES
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 BROSELOW?

The registered manufacturer of record for BROSELOW is AIRLIFE.

What is the Primary UDI-DI identifier for BROSELOW?

The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 7700WAW.

What classification code is assigned to this device?

This device is registered under product classification code OKI.

Similar Classification Devices (OKI)

Other Devices by AIRLIFE

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