FDA UDI In Commercial Distribution 🇺🇸 United States

MLCL Upgrade

DI: 00195278940193 · Model: AltiX AI.i · Ge Medical Systems Information Technologies, Inc.
Product Codes
1
GMDN Terms
2
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
MLCL Upgrade
Primary DI
00195278940193
Version / Model
AltiX AI.i
Catalog Number
5973644
Company Name
Ge Medical Systems Information Technologies, Inc.
Labeler DUNS
118935631
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2025-05-05
Public Version
1
Public Version Date
2025-05-13
Public Version Status
New
Public Device Record Key
c2a99c4c-0518-498d-b154-dcff5e137467

Device Description

Upgrade Kit MLCL V9.0

Device Characteristics

Single Use
No
Prescription Use (Rx)
Yes
Over the Counter (OTC)
No
Kit
No
Combination Product
No
HCT/P
No
Contains NRL
No
Not Made with NRL
No
MRI Safety
Labeling does not contain MRI Safety Information
Direct Marking Exempt
No
PM Exempt
No
Has Serial Number
No
Has Lot/Batch Number
Yes
Has Manufacturing Date
No
Has Expiration Date
No
Has Donation ID
No

Sterilization

Is Sterile
No
Sterilization Prior Use
No

Product Codes

Code Name
DQK Computer, Diagnostic, Programmable

GMDN Terms

Code Name
17898 Cardiac electrophysiology analysis system
37807 Cardiac catheterization monitoring system

Identifiers

Type ID
Primary 00195278940193

Premarket Submissions

Submission Number Supplement Number
K243540 000