Primary Device ID | 07290012672019 |
NIH Device Record Key | ea5dcbf1-cc31-4e76-b06f-d69636d31fcd |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | Commwell |
Version Model Number | ES-ECG System |
Catalog Number | 5-045-00 |
Company DUNS | 532013976 |
Company Name | COMMWELL RESEARCH & DEVELOPMENT LTD. |
Device Count | 1 |
DM Exempt | false |
Pre-market Exempt | false |
MRI Safety Status | Labeling does not contain MRI Safety Information |
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 | true |
OTC Over-The-Counter | false |
Device Issuing Agency | Device ID |
---|---|
GS1 | 07290012672019 [Primary] |
DRX | Electrode, Electrocardiograph |
Steralize Prior To Use | false |
Device Is Sterile | false |
Public Version Status | Update |
Device Record Status | Published |
Public Version Number | 3 |
Public Version Date | 2018-07-06 |
Device Publish Date | 2017-01-25 |
07290012672064 | ECG Mgmt Sys with ECG Analysis |
07290012672057 | An instrument designed to measure electrical potentials on the body surface to generate a record |
07290012672026 | An instrument designed to measure electrical potentials on the body surface to generate a record |
07290012672019 | An instrument designed to measure electrical potentials on the body surface to generate a record |