FDA UDI In Commercial Distribution 🇺🇸 United States

Us2.ca

DI: 00860005876891 · Model: 1 · EKO.AI PTE. LTD.
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
Us2.ca
Primary DI
00860005876891
Version / Model
1
Company Name
EKO.AI PTE. LTD.
Labeler DUNS
659454378
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2026-04-20
Public Version
1
Public Version Date
2026-04-28
Public Version Status
New
Public Device Record Key
7fd849a3-d97e-4e42-b788-ad65d808821b

Device Description

Us2.ca processes acquired transthoracic cardiac ultrasound images to support qualified cardiologists, sonographers, or other licensed professional healthcare practitioners in their diagnosis of cardiac amyloidosis. Us2.ca is intended for use only in adult patients with increased left ventricular wall thickness, defined as an interventricular septal thickness (IVSd) or left ventricular posterior wall thickness (LVPWd) > 12mm. Us2.ca is not intended to provide a diagnosis and does not replace current standards of care. The results from Us2.ca are not intended to exclude the need for further follow-up on cardiac amyloidosis.

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
No
Has Expiration Date
No
Has Donation ID
No

Sterilization

Is Sterile
No
Sterilization Prior Use
No

Product Codes

Code Name
SDJ Adjunctive Cardiac Amyloidosis Status Indicator

GMDN Terms

Code Name
57812 Radiology DICOM image processing application software

Identifiers

Type ID
Primary 00860005876891

Premarket Submissions

Submission Number Supplement Number
K250151 000