| Primary Device ID | 00382903390113 |
| NIH Device Record Key | ce8c80da-e2c7-4d32-a752-3db6052665ec |
| Commercial Distribution Status | In Commercial Distribution |
| Brand Name | BD FACSCount™ |
| Version Model Number | 339011 |
| Catalog Number | 339011 |
| Company DUNS | 024230633 |
| Company Name | BECTON, DICKINSON AND COMPANY |
| 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 | 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 |
| Phone | +1(877)232-8995 |
| BDBCustomerService@bd.com | |
| Phone | +1(877)232-8995 |
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| BDBCustomerService@bd.com |
| Device Issuing Agency | Device ID |
|---|---|
| GS1 | 00382903390113 [Primary] |
| GKZ | Counter, differential cell |
| Steralize Prior To Use | false |
| Device Is Sterile | false |
| Public Version Status | Update |
| Device Record Status | Published |
| Public Version Number | 3 |
| Public Version Date | 2018-07-06 |
| Device Publish Date | 2016-06-23 |
| 00382903446193 | BD FACSCount System Users Guide and Software |
| 00382903401673 | BD FACSCount Reagent Kit 50 Tests IVD |
| 00382903401666 | BD FACSCount Control Kit 25 Tests IVD |
| 00382903390113 | FACSCount CD4 Users Guide and Software |
| 00382903390106 | BD FACSCount CD4 Reagent Kit 50 Tests |
| 00382903378586 | BD FACSCount Instrument System |