Primary Device ID | 00815871020862 |
NIH Device Record Key | f6a00301-9de7-4cbc-9090-9735ea32c3ae |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | True ECG Advance |
Version Model Number | 60137 |
Company DUNS | 178440426 |
Company Name | Avante |
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 | false |
OTC Over-The-Counter | false |
Phone | 502-244-4444 |
devicehelp@dremed.com | |
Phone | 502-244-4444 |
devicehelp@dremed.com | |
Phone | 502-244-4444 |
devicehelp@dremed.com | |
Phone | 502-244-4444 |
devicehelp@dremed.com | |
Phone | 502-244-4444 |
devicehelp@dremed.com | |
Phone | 502-244-4444 |
devicehelp@dremed.com | |
Phone | 502-244-4444 |
devicehelp@dremed.com | |
Phone | 502-244-4444 |
devicehelp@dremed.com | |
Phone | 502-244-4444 |
devicehelp@dremed.com | |
Phone | 502-244-4444 |
devicehelp@dremed.com | |
Phone | 502-244-4444 |
devicehelp@dremed.com | |
Phone | 502-244-4444 |
devicehelp@dremed.com |
Device Issuing Agency | Device ID |
---|---|
GS1 | 00815871020862 [Primary] |
DPS | Electrocardiograph |
Steralize Prior To Use | false |
Device Is Sterile | false |
Public Version Status | Update |
Device Record Status | Published |
Public Version Number | 4 |
Public Version Date | 2019-06-19 |
Device Publish Date | 2016-09-23 |
00815871020879 | 60137ADVS |
00815871020862 | 60137 |
00815871020855 | 60137ADV |