gudid
Primary ID: 80-1999
NAR (UDI 80-1999)
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 80-1999
Device Regulatory Overview
The NAR (Model/Catalog Number: 80-1999) 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
- 80-1999
- Product Code / EMDN
- OHO
- 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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Get API Token Access ($49/mo)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 80-1999.
What classification code is assigned to this device?
This device is registered under product classification code OHO.
Similar Classification Devices (OHO)
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