FDA UDI In Commercial Distribution 🇺🇸 United States

CardioLab

DI: 00195278935656 · Model: AltiX AI.i · Ge Medical Systems Information Technologies, Inc.
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

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Basic Information

Brand Name
CardioLab
Primary DI
00195278935656
Version / Model
AltiX AI.i
Catalog Number
2400000-004
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
fb098b5d-01b9-44d2-95cb-8fc0cfa68abe

Device Description

AltiX AI.i CardioLab Computer

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
Yes
Has Lot/Batch Number
No
Has Manufacturing Date
Yes
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

Identifiers

Type ID
Primary 00195278935656

Premarket Submissions

Submission Number Supplement Number
K243540 000