GUDIDData
gudid Primary ID: MCCB0524

Atlas Medical Oss Matrix+ (UDI MCCB0524)

Manufactured by Biogennix, LLC

Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for Atlas Medical Oss Matrix+ - Primary ID MCCB0524

Device Regulatory Overview

The Atlas Medical Oss Matrix+ (Model/Catalog Number: MCCB0524) is a medical device manufactured by Biogennix, LLC. This product is indexed under FDA Product Code / Category Classification KGN within international Unique Device Identification (UDI) compliance databases.

Technical Specifications

Model Number
MCCB0524
Product Code / EMDN
KGN
Device Name
Database Sync Date
2026-08-09 09:43:40

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 Atlas Medical Oss Matrix+?

The registered manufacturer of record for Atlas Medical Oss Matrix+ is Biogennix, LLC.

What is the Primary UDI-DI identifier for Atlas Medical Oss Matrix+?

The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is MCCB0524.

What classification code is assigned to this device?

This device is registered under product classification code KGN.

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