| Primary Device ID | 50382903667043 |
| NIH Device Record Key | c6097481-5c0e-4bb9-842d-22b8529cada1 |
| Commercial Distribution Status | In Commercial Distribution |
| Brand Name | BD Vacutainer® No Additive |
| Version Model Number | 366704 |
| Catalog Number | 366704 |
| Company DUNS | 001292192 |
| Company Name | BECTON, DICKINSON AND COMPANY |
| Device Count | 1000 |
| DM Exempt | false |
| Pre-market Exempt | true |
| MRI Safety Status | Labeling does not contain MRI Safety Information |
| Human Cell/Tissue Product | false |
| Device Kit | false |
| Device Combination Product | false |
| Single Use | true |
| Lot Batch | true |
| Serial Number | false |
| Manufacturing Date | false |
| Expiration Date | true |
| Donation Id Number | false |
| Contains Natural Rubber Latex | false |
| Labeled No Natural Rubber Latex | false |
| RX Perscription | true |
| OTC Over-The-Counter | false |
| Device Issuing Agency | Device ID |
|---|---|
| GS1 | 00382903667048 [Unit of Use] |
| GS1 | 50382903667043 [Primary] |
| FMH | CONTAINER, SPECIMEN, STERILE |
| Steralize Prior To Use | false |
| Device Is Sterile | true |
| Public Version Status | Update |
| Device Record Status | Published |
| Public Version Number | 2 |
| Public Version Date | 2018-03-29 |
| Device Publish Date | 2016-07-28 |
| 50382903667043 | BD Vacutainer® No Additive |
| 50382903667036 | BD Vacutainer® No Additive |
Mark Image Registration | Serial | Company Trademark Application Date |
|---|---|
![]() BD VACUTAINER 78264506 2858038 Live/Registered |
Becton, Dickinson and Company 2003-06-19 |
![]() BD VACUTAINER 77000481 3257557 Dead/Cancelled |
Becton, Dickinson and Company 2006-09-15 |