FDA UDI In Commercial Distribution 🇺🇸 United States

CORE 500 Digital Stethoscope - Ruby Chestpiece

DI: 00850010298740 · Model: E8 · Eko Devices, Inc.
Product Codes
2
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
CORE 500 Digital Stethoscope - Ruby Chestpiece
Primary DI
00850010298740
Version / Model
E8
Catalog Number
COR500_RED
Company Name
Eko Devices, Inc.
Labeler DUNS
079670921
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2025-10-15
Public Version
1
Public Version Date
2025-10-23
Public Version Status
New
Public Device Record Key
880d1245-fc0d-4ebc-ae24-d76de726872b

Device Description

The CORE 500™ Digital Stethoscope is intended to be used by clinicians or lay users to electronically amplify, filter, and transfer body sounds and three lead electrocardiogram (ECG) waveforms. The CORE 500™ Digital Stethoscope also displays ECG waveforms and heart rate on the display and accompanying mobile application (when prescribed or used under the care of a clinician or by lay users). A lay user is not intended to interpret or take clinical action based on the device output without consulting with a qualified healthcare professional.

Device Characteristics

Single Use
No
Prescription Use (Rx)
No
Over the Counter (OTC)
Yes
Kit
No
Combination Product
No
HCT/P
No
Contains NRL
No
Not Made with NRL
No
MRI Safety
MR Unsafe
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
DPS Electrocardiograph
DQD Stethoscope, Electronic

GMDN Terms

Code Name
13754 Electronic acoustic stethoscope

Identifiers

Type ID
Primary 00850010298740

Premarket Submissions

Submission Number Supplement Number
K233609 000