| Primary Device ID | 50382903686082 |
| NIH Device Record Key | 5451bd8e-7edc-4628-9b05-d84080768fa5 |
| Commercial Distribution Status | In Commercial Distribution |
| Brand Name | Becton Dickinson and Company, USA 22G x 1 1/4 |
| Version Model Number | 368608 |
| Catalog Number | 368608 |
| Company DUNS | 001292192 |
| Company Name | BECTON, DICKINSON AND COMPANY |
| Device Count | 480 |
| 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 | 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 | 00382903686087 [Unit of Use] |
| GS1 | 50382903686082 [Primary] |
| FMI | Needle, hypodermic, single lumen |
| Steralize Prior To Use | false |
| Device Is Sterile | true |
| Public Version Status | Update |
| Device Record Status | Published |
| Public Version Number | 4 |
| Public Version Date | 2019-01-08 |
| Device Publish Date | 2016-07-28 |
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