Primary Device ID | 00850010298412 |
NIH Device Record Key | 3c5f8c6f-57a8-464c-9c75-e564a8263950 |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | CORE 500 Digital Stethoscope - Champagne Chestpiece |
Version Model Number | E8 |
Catalog Number | COR500_CHP |
Company DUNS | 079670921 |
Company Name | Eko Devices, Inc. |
Device Count | 1 |
DM Exempt | false |
Pre-market Exempt | false |
MRI Safety Status | MR Unsafe |
Human Cell/Tissue Product | false |
Device Kit | false |
Device Combination Product | false |
Single Use | false |
Lot Batch | false |
Serial Number | true |
Manufacturing Date | true |
Expiration Date | false |
Donation Id Number | false |
Contains Natural Rubber Latex | false |
Labeled No Natural Rubber Latex | false |
RX Perscription | false |
OTC Over-The-Counter | true |
Device Issuing Agency | Device ID |
---|---|
GS1 | 00850010298412 [Primary] |
DPS | Electrocardiograph |
Steralize Prior To Use | false |
Device Is Sterile | false |
Public Version Status | New |
Device Record Status | Published |
Public Version Number | 1 |
Public Version Date | 2025-03-20 |
Device Publish Date | 2025-03-12 |