gudid Primary ID: 536757-NB

MGC Diagnostics (UDI 536757-NB)

Manufactured by MEDICAL GRAPHICS CORPORATION

Data verified against official FDA/EUDAMED records on August 9, 2026

Scannable UDI-DI Representation

Device Regulatory Overview

The MGC Diagnostics (Model/Catalog Number: 536757-NB) is a medical device manufactured by MEDICAL GRAPHICS CORPORATION. This product is indexed under FDA Product Code / Category Classification BZG within international Unique Device Identification (UDI) compliance databases.

Technical Specifications

Model Number: 536757-NB
Product Code / EMDN: BZG
Device Name: PREVENT II FILTER-ROUND-BLUE
Database Sync Date: 2026-08-09 09:17:09

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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Frequently Asked Questions

Who is the primary manufacturer of MGC Diagnostics?

The registered manufacturer of record for MGC Diagnostics is MEDICAL GRAPHICS CORPORATION.

What is the Primary UDI-DI identifier for MGC Diagnostics?

The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 536757-NB.

What classification code is assigned to this device?

This device is registered under product classification code BZG.

Similar Classification Devices (BZG)

Other Devices by MEDICAL GRAPHICS CORPORATION

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