| Primary Device ID | 00842209100026 |
| NIH Device Record Key | 586fd400-24b9-4f44-9035-dc9930ba27c9 |
| Commercial Distribution Status | In Commercial Distribution |
| Brand Name | Sharps container |
| Version Model Number | 30-0014 |
| Catalog Number | 30-0014 |
| Company DUNS | 832426782 |
| Company Name | NORTH AMERICAN RESCUE, LLC |
| 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 | true |
| Device Issuing Agency | Device ID |
|---|---|
| GS1 | 00842209100026 [Primary] |
| GS1 | 00842209100033 [Package] Package: box [6 Units] In Commercial Distribution |
| GS1 | 00842209101375 [Package] Package: box [200 Units] In Commercial Distribution |
| MMK | Container, Sharps |
| Steralize Prior To Use | false |
| Device Is Sterile | false |
| Public Version Status | Update |
| Device Record Status | Published |
| Public Version Number | 6 |
| Public Version Date | 2019-08-27 |
| Device Publish Date | 2016-09-22 |
| 00842209133307 - NAR | 2024-11-15 |
| 00842209133314 - NAR | 2024-11-15 |
| 00842209133321 - NAR | 2024-11-15 |
| 00842209133338 - NAR | 2024-11-15 |
| 00842209133345 - NAR | 2024-11-15 |
| 00842209133352 - NAR | 2024-11-15 |
| 00842209133369 - NAR | 2024-11-15 |
| 00842209133376 - NAR | 2024-11-15 |