FDA UDI In Commercial Distribution 🇺🇸 United States

EchoGo

DI: 05060634690058 · Model: Heart Failure 2.0 · ULTROMICS LIMITED
Product Codes
1
GMDN Terms
3
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
EchoGo
Primary DI
05060634690058
Version / Model
Heart Failure 2.0
Company Name
ULTROMICS LIMITED
Labeler DUNS
222850684
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2024-12-17
Public Version
1
Public Version Date
2024-12-25
Public Version Status
New
Public Device Record Key
5855f3e0-4b54-4897-8718-13356b71134e

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
Yes
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
Yes
Has Expiration Date
No
Has Donation ID
No

Sterilization

Is Sterile
No
Sterilization Prior Use
No

Product Codes

Code Name
QUO Adjunctive Heart Failure Status Indicator

GMDN Terms

Code Name
40873 Ultrasound imaging system application software
44783 Cardiac mapping system application software
57812 Radiology DICOM image processing application software

Identifiers

Type ID
Primary 05060634690058

Premarket Submissions

Submission Number Supplement Number
K240013 000