FDA UDI In Commercial Distribution 🇺🇸 United States

Eko CORE 500 Digital Stethoscope Chestpiece

DI: 00850010298160 · Model: COR500 · Eko Devices, Inc.
Product Codes
2
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
Eko CORE 500 Digital Stethoscope Chestpiece
Primary DI
00850010298160
Version / Model
COR500
Catalog Number
COR500
Company Name
Eko Devices, Inc.
Labeler DUNS
079670921
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2023-07-10
Public Version
1
Public Version Date
2023-07-18
Public Version Status
New
Public Device Record Key
13a019cd-920b-4f10-a623-13d1beb8aaed

Device Description

Eko CORE 500 Digital Stethoscope Chestpiece

Device Characteristics

Single Use
No
Prescription Use (Rx)
No
Over the Counter (OTC)
No
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
DQD Stethoscope, Electronic
DPS Electrocardiograph

GMDN Terms

Code Name
13754 Electronic stethoscope

Identifiers

Type ID
Primary 00850010298160

Premarket Submissions

Submission Number Supplement Number
K230111 000