MLCL Client Software (UDI AltiX AI.i)
Manufactured by Ge Medical Systems Information Technologies, Inc.
Device Regulatory Overview
The MLCL Client Software (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
- Software Medical Device GE Client Software V9.0
- Database Sync Date
- 2026-08-09 09:14:30
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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Get API Token Access ($49/mo)Frequently Asked Questions
Who is the primary manufacturer of MLCL Client Software?
The registered manufacturer of record for MLCL Client Software is Ge Medical Systems Information Technologies, Inc..
What is the Primary UDI-DI identifier for MLCL Client Software?
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.
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