gudid Primary ID: AltiX AI.i

MLCL Upgrade (UDI AltiX AI.i)

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 MLCL Upgrade (Model/Catalog Number: AltiX AI.i) 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: AltiX AI.i
Product Code / EMDN: DQK
Device Name: Upgrade Kit MLCL V9.0
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 MLCL Upgrade?

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

What is the Primary UDI-DI identifier for MLCL Upgrade?

The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is AltiX AI.i.

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