Primary Device ID | 15099590381646 |
NIH Device Record Key | e22a85c7-0903-42ed-9c20-70ee64d20ba6 |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | UniCel DxH |
Version Model Number | 800 |
Catalog Number | 629029, B66445 |
Company DUNS | 008254708 |
Company Name | Beckman Coulter, 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 | 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 |