BROSELOW (UDI 7700OIO)

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: 7700OIO) 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: 7700OIO
Product Code / EMDN: OKI
Device Name: BROSELOW INTRAOSSEOUS MODULES
Database Sync Date: 2026-08-09 09:16:32

Full Regulatory Attributes

🔒 Token Gated

{
    "review_panel": "AN",
    "gudid_di_status": "Published",
    "sterilization_methods": ["EO", "Gamma"],
    "rx_only": true
}

Unlock Compliance Data & Serialization Specs

Access raw JSON payloads, UDI-DI packaging hierarchies, and Notified Body IDs.

Get API Token Access ($49/mo)

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 7700OIO.

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

Programmatic Export

Export this master device record as standardized JSON or CSV for compliance audits.

JSON API Endpoint