GUDIDData
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gudid Primary ID: 08321248 190

OXY Oxycodone (UDI 08321248 190)

Manufactured by Microgenics Corporation

Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for OXY Oxycodone - Primary ID 08321248 190

Device Regulatory Overview

The OXY Oxycodone (Model/Catalog Number: 08321248 190) is a medical device manufactured by Microgenics Corporation. This product is indexed under FDA Product Code / Category Classification DJG within international Unique Device Identification (UDI) compliance databases.

ACTIVE SAFETY RECALL ALERT 3 Event(s) Found

Enforcement actions are currently active for this product line.

ID: Z-1284-2022 View Full Alert →

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🔒 Compromised Lot & Serial Numbers Locked
Verify if facility inventory is affected by this recall.
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ID: Z-1563-2013 View Full Alert →

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ID: Z-0379-2013 View Full Alert →

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🔒 Compromised Lot & Serial Numbers Locked
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Unlock Lot Data ($49)

Technical Specifications

Model Number
08321248 190
Product Code / EMDN
DJG
Device Name
Database Sync Date
2026-08-09 09:44:46

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 OXY Oxycodone?

The registered manufacturer of record for OXY Oxycodone is Microgenics Corporation.

What is the Primary UDI-DI identifier for OXY Oxycodone?

The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 08321248 190.

What classification code is assigned to this device?

This device is registered under product classification code DJG.

Similar Classification Devices (DJG)

Other Devices by Microgenics Corporation

Programmatic Export

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

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