GUDIDData
gudid Primary ID: 7600PA

Nonin (UDI 7600PA)

Manufactured by NONIN MEDICAL, INC.

Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for Nonin - Primary ID 7600PA

Device Regulatory Overview

The Nonin (Model/Catalog Number: 7600PA) is a medical device manufactured by NONIN MEDICAL, INC.. This product is indexed under FDA Product Code / Category Classification MUD within international Unique Device Identification (UDI) compliance databases.

Technical Specifications

Model Number
7600PA
Product Code / EMDN
MUD
Device Name
7600 PA Regional
Database Sync Date
2026-08-09 09:33:17

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 Nonin?

The registered manufacturer of record for Nonin is NONIN MEDICAL, INC..

What is the Primary UDI-DI identifier for Nonin?

The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 7600PA.

What classification code is assigned to this device?

This device is registered under product classification code MUD.

Programmatic Export

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

JSON API Endpoint