GUDIDData
gudid Primary ID: 80-1993

NAR (UDI 80-1993)

Manufactured by NORTH AMERICAN RESCUE, LLC

Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for NAR - Primary ID 80-1993

Device Regulatory Overview

The NAR (Model/Catalog Number: 80-1993) is a medical device manufactured by NORTH AMERICAN RESCUE, LLC. This product is indexed under FDA Product Code / Category Classification OHO within international Unique Device Identification (UDI) compliance databases.

Technical Specifications

Model Number
80-1993
Product Code / EMDN
OHO
Device Name
Database Sync Date
2026-08-09 09:13:29

Full Regulatory Attributes

🔒 Token Gated
{
    "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 80-1993.

What classification code is assigned to this device?

This device is registered under product classification code OHO.

Programmatic Export

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