Primary Device ID | 80010939120010 |
NIH Device Record Key | 0ec9660b-8a15-4b1a-8d65-6662c8bcd13e |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | Conserus Enterprise Viewer |
Version Model Number | 1.1 |
Company DUNS | 962049362 |
Company Name | MCKESSON TECHNOLOGIES INC. |
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 | true |
Lot Batch | true |
Serial Number | false |
Manufacturing Date | false |
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 |