NAR (UDI 60-0027)

Manufactured by NORTH AMERICAN RESCUE, LLC

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

Scannable UDI-DI Representation

Device Regulatory Overview

The NAR (Model/Catalog Number: 60-0027) is a medical device manufactured by NORTH AMERICAN RESCUE, LLC. This product is indexed under FDA Product Code / Category Classification FPP within international Unique Device Identification (UDI) compliance databases.

Technical Specifications

Model Number: 60-0027
Product Code / EMDN: FPP
Device Name
Database Sync Date: 2026-08-09 09:13:29

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 NAR?

The registered manufacturer of record for NAR is NORTH AMERICAN RESCUE, LLC.

What is the Primary UDI-DI identifier for NAR?

The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 60-0027.

What classification code is assigned to this device?

This device is registered under product classification code FPP.

Similar Classification Devices (FPP)

Other Devices by NORTH AMERICAN RESCUE, LLC

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