Primary Device ID | 15099590512118 |
NIH Device Record Key | ca37db72-627b-432f-bd8b-b4a0fff47748 |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | Navios Analysis Software |
Version Model Number | 774952 |
Catalog Number | 774952 |
Company DUNS | 985071975 |
Company Name | BECKMAN COULTER IRELAND 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 | false |
Lot Batch | false |
Serial Number | false |
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 |