gudid Primary ID: 5 A5

MAC (UDI 5 A5)

Manufactured by Ge Medical Systems Information Technologies, Inc.

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

Scannable UDI-DI Representation

Device Regulatory Overview

The MAC (Model/Catalog Number: 5 A5) is a medical device manufactured by Ge Medical Systems Information Technologies, Inc.. This product is indexed under FDA Product Code / Category Classification DQK within international Unique Device Identification (UDI) compliance databases.

Technical Specifications

Model Number: 5 A5
Product Code / EMDN: DQK
Device Name: MAC 5 A5
Database Sync Date: 2026-08-09 09:14:30

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 MAC?

The registered manufacturer of record for MAC is Ge Medical Systems Information Technologies, Inc..

What is the Primary UDI-DI identifier for MAC?

The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 5 A5.

What classification code is assigned to this device?

This device is registered under product classification code DQK.

Similar Classification Devices (DQK)

Other Devices by Ge Medical Systems Information Technologies, Inc.

Programmatic Export

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

JSON API Endpoint