Primary Device ID | 06944413808072 |
NIH Device Record Key | 1785a431-658c-4831-9a81-15b0e15d2dda |
Commercial Distribution Status | In Commercial Distribution |
Version Model Number | Insight |
Company DUNS | 529173163 |
Company Name | Edan Instruments, Inc. |
Device Count | 1 |
DM Exempt | false |
Pre-market Exempt | true |
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 | 06944413808072 [Primary] |
NSX | Software, Transmission And Storage, Patient Data |
Steralize Prior To Use | false |
Device Is Sterile | false |
Public Version Status | Update |
Device Record Status | Published |
Public Version Number | 3 |
Public Version Date | 2018-05-08 |
Device Publish Date | 2016-09-21 |
06944413815889 - Patient Monitor | 2024-06-25 |
06944413815896 - Patient Monitor | 2024-06-25 |
06944413815902 - Patient Monitor | 2024-06-25 |
06944413813977 - ECG cable | 2024-06-06 |
06944413813984 - ECG cable | 2024-06-06 |
06944413813991 - ECG cable | 2024-06-06 |
06944413814004 - ECG cable | 2024-06-06 |
06944413814011 - ECG cable | 2024-06-06 |