| Primary Device ID | 10884450012656 |
| NIH Device Record Key | 3891f877-4295-4d30-93c5-a34ea13705e4 |
| Commercial Distribution Status | In Commercial Distribution |
| Brand Name | Merit S-MAK™ |
| Version Model Number | 00884450012659 |
| Catalog Number | S-MAK501N-15/A |
| 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 | true |
| 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 |
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| Device Size Text, specify | 0 |
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| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
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| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Device Issuing Agency | Device ID |
|---|---|
| GS1 | 00884450012659 [Primary] |
| GS1 | 10884450012656 [Package] Contains: 00884450012659 Package: [10 Units] In Commercial Distribution |
| DRE | DILATOR, VESSEL, FOR PERCUTANEOUS CATHETERIZATION |
| 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 | 2016-09-24 |
| 10884450155070 | 00884450155073 |
| 10884450155063 | 00884450155066 |
| 10884450155049 | 00884450155042 |
| 10884450144463 | 00884450144466 |
| 10884450144456 | 00884450144459 |
| 10884450144449 | 00884450144442 |
| 10884450144432 | 00884450144435 |
| 10884450013295 | 00884450013298 |
| 10884450013288 | 00884450013281 |
| 10884450013271 | 00884450013274 |
| 10884450012861 | 00884450012864 |
| 10884450012663 | 00884450012666 |
| 10884450012656 | 00884450012659 |
| 10884450012649 | 00884450012642 |
| 10884450012632 | 00884450012635 |
| 10884450012625 | 00884450012628 |
| 10884450012618 | 00884450012611 |
| 10884450410438 | 00884450410431 |
| 10884450847357 | C |
| 10884450860356 | T |
| 10884450847340 | F |