Primary Device ID | 14987666545072 |
NIH Device Record Key | 17d72d5e-5924-4016-b604-951c51144192 |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | DxC 500i Clinical Analyzer, DxC 500i AU Chemistry Module |
Version Model Number | C65321 |
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 |