| Primary Device ID | 20884450008236 |
| NIH Device Record Key | 58ec314b-7781-4d7e-a744-b9248f1b1114 |
| Commercial Distribution Status | In Commercial Distribution |
| Brand Name | Merit Disposal Depot™ |
| Version Model Number | 00884450008232 |
| Catalog Number | MDD220H/B |
| Company DUNS | 184763290 |
| Company Name | Merit Medical Systems, 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 | true |
| Donation Id Number | false |
| Contains Natural Rubber Latex | false |
| Labeled No Natural Rubber Latex | false |
| RX Perscription | false |
| OTC Over-The-Counter | false |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Device Issuing Agency | Device ID |
|---|---|
| GS1 | 00884450008232 [Primary] |
| GS1 | 10884450008239 [Package] Contains: 00884450008232 Package: [20 Units] In Commercial Distribution |
| GS1 | 20884450008236 [Package] Contains: 10884450008239 Package: [4 Units] In Commercial Distribution |
| DQO | CATHETER, INTRAVASCULAR, DIAGNOSTIC |
| Steralize Prior To Use | false |
| Device Is Sterile | true |
| Public Version Status | Update |
| Device Record Status | Published |
| Public Version Number | 3 |
| Public Version Date | 2018-07-06 |
| Device Publish Date | 2016-09-26 |
| 10884450123130 | 00884450123133 |
| 20884450050105 | 00884450050101 |
| 20884450028579 | 00884450028575 |
| 10884450024451 | 00884450024454 |
| 20884450024403 | 00884450024409 |
| 10884450023676 | 00884450023679 |
| 20884450022850 | 00884450022856 |
| 20884450022089 | 00884450022085 |
| 20884450019607 | 00884450019603 |
| 20884450013421 | 00884450013427 |
| 20884450008236 | 00884450008232 |
| 20884450008229 | 00884450008225 |
| 10884450419769 | 00884450419762 |
| 20884450504936 | 00884450504932 |
| 10884450790714 | Initial Release |
| 10884450862893 | T |
| 10884450862855 | T |
| 20884450862845 | T |
| 10884450862879 | T |
| 10884450862862 | T |
| 10884450000004 | T |
| 10884450093426 | Initial Release |