| Primary Device ID | 00990013400112 |
| NIH Device Record Key | 6457d4d6-6812-4332-82c7-baf9a935003d |
| Commercial Distribution Status | In Commercial Distribution |
| Brand Name | BD |
| Version Model Number | 304456 |
| Catalog Number | 259868 |
| Company DUNS | 253548978 |
| Company Name | Keter Canada 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 | true |
| 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 |
| Device Issuing Agency | Device ID |
|---|---|
| GS1 | 00990013400112 [Primary] |
| MMK | Container, Sharps |
| Steralize Prior To Use | false |
| Device Is Sterile | false |
| Public Version Status | New |
| Device Record Status | Published |
| Public Version Number | 1 |
| Public Version Date | 2024-05-23 |
| Device Publish Date | 2024-05-15 |
| 00990013400136 | Becton Dickinson - AP 30 DUO BLACK |
| 00990013400129 | Becton Dickinson - AP 30 DUO WHITE |
| 00990013400112 | Becton Dickinson - AP 30 DUO YELLOW |
| 00990013400105 | Becton Dickinson - AP 30 DUO RED |
| 00990013400099 | Becton Dickinson - AP 60 DUO BLACK |
| 00990013400082 | Becton Dickinson - AP 60 DUO WHITE |
| 00990013400075 | Becton Dickinson - AP 60 DUO YELLOW |
| 00990013400068 | Becton Dickinson - AP 60 DUO RED |