| Primary Device ID | 15099590694982 |
| NIH Device Record Key | 820728c8-91d0-4042-b8bf-790f64afbc5f |
| Commercial Distribution Status | In Commercial Distribution |
| Brand Name | ClearLLab 10C |
| Version Model Number | B99883 |
| 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 | true |
| Serial Number | true |
| Manufacturing Date | true |
| Expiration Date | true |
| Donation Id Number | false |
| Contains Natural Rubber Latex | false |
| Labeled No Natural Rubber Latex | false |
| RX Perscription | false |
| OTC Over-The-Counter | false |
| Device Issuing Agency | Device ID |
|---|---|
| GS1 | 15099590694982 [Primary] |
| PWD | Flow Cytometric Test System For Hematopoietic Neoplasms |
| Steralize Prior To Use | false |
| Device Is Sterile | false |
| Public Version Status | New |
| Device Record Status | Published |
| Public Version Number | 1 |
| Public Version Date | 2019-04-03 |
| Device Publish Date | 2019-03-26 |
| 15099590701505 | ClearLLab 10C M2 Cell Tube |
| 15099590701499 | ClearLLab 10C M1 Cell Tube |
| 15099590701482 | ClearLLab 10C T Cell Tube |
| 15099590701475 | ClearLLab 10C B Cell Tube |
| 15099590694982 | ClearLLab Compensation Beads |
| 15099590694975 | ClearLLab Control Cells abnormal |
| 15099590694968 | ClearLLab 10C Control Cells normal |