gudid Primary ID: 24500

3M Ranger (UDI 24500)

Manufactured by 3M COMPANY

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

Scannable UDI-DI Representation

Device Regulatory Overview

The 3M Ranger (Model/Catalog Number: 24500) is a medical device manufactured by 3M COMPANY. This product is indexed under FDA Product Code / Category Classification BSB within international Unique Device Identification (UDI) compliance databases.

Technical Specifications

Model Number: 24500
Product Code / EMDN: BSB
Device Name: 3M Ranger Blood/Fluid Warming Unit, 24500, 120V-ENG-B, 1 Each
Database Sync Date: 2026-08-09 09:04:13

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 3M Ranger?

The registered manufacturer of record for 3M Ranger is 3M COMPANY.

What is the Primary UDI-DI identifier for 3M Ranger?

The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 24500.

What classification code is assigned to this device?

This device is registered under product classification code BSB.

Similar Classification Devices (BSB)

Other Devices by 3M COMPANY

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