GUDIDData
gudid Primary ID: P080023

Pro Advantage (UDI P080023)

Manufactured by NATIONAL DISTRIBUTION & CONTRACTING, INC.

Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for Pro Advantage - Primary ID P080023

Device Regulatory Overview

The Pro Advantage (Model/Catalog Number: P080023) is a medical device manufactured by NATIONAL DISTRIBUTION & CONTRACTING, INC.. This product is indexed under FDA Product Code / Category Classification JHI within international Unique Device Identification (UDI) compliance databases.

Technical Specifications

Model Number
P080023
Product Code / EMDN
JHI
Device Name
Pro Advantage Test Strips HCG Urine 100/BX
Database Sync Date
2026-08-09 09:14:43

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 Pro Advantage?

The registered manufacturer of record for Pro Advantage is NATIONAL DISTRIBUTION & CONTRACTING, INC..

What is the Primary UDI-DI identifier for Pro Advantage?

The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is P080023.

What classification code is assigned to this device?

This device is registered under product classification code JHI.

Programmatic Export

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

JSON API Endpoint