| Primary Device ID | 10884450007140 |
| NIH Device Record Key | e01ad6af-de71-4ca0-8f2f-7b2e4b76c3ef |
| Commercial Distribution Status | In Commercial Distribution |
| Brand Name | MBA™ |
| Version Model Number | 00884450007143 |
| Catalog Number | MAP403/B |
| Company DUNS | 184763290 |
| Company Name | Merit Medical Systems, Inc. |
| Device Count | 1 |
| 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 | false |
| OTC Over-The-Counter | false |
| Device Issuing Agency | Device ID |
|---|---|
| GS1 | 00884450007143 [Primary] |
| GS1 | 10884450007140 [Package] Contains: 00884450007143 Package: [25 Units] In Commercial Distribution |
| GS1 | 20884450007147 [Package] Package: [4 Units] In Commercial Distribution |
| DTL | Adaptor, stopcock, manifold, fitting, cardiopulmonary bypass |
| Steralize Prior To Use | false |
| Device Is Sterile | true |
| Public Version Status | Update |
| Device Record Status | Published |
| Public Version Number | 3 |
| Public Version Date | 2020-03-05 |
| Device Publish Date | 2016-09-24 |
| 10884450028558 | 00884450028551 |
| 10884450024437 | 00884450024430 |
| 20884450008540 | 00884450008546 |
| 10884450007140 | 00884450007143 |
| 10884450651121 | 00884450651124 |
| 20884450650701 | 00884450650707 |
| 10884450668747 | A |
| 20884450818101 | C |