| Primary Device ID | 10884450569266 |
| NIH Device Record Key | de262adb-9108-4b60-ac23-0ded8cf8123b |
| Commercial Distribution Status | In Commercial Distribution |
| Brand Name | Pressure Monitor Tubing |
| Version Model Number | 00884450569269 |
| Catalog Number | PM6024/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 | 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 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 | 00884450569269 [Primary] |
| GS1 | 10884450569266 [Package] Contains: 00884450569269 Package: [25 Units] In Commercial Distribution |
| GS1 | 20884450569263 [Package] Package: [4 Units] In Commercial Distribution |
| DXJ | DISPLAY, CATHODE-RAY TUBE, MEDICAL |
| FPK | Tubing, fluid delivery |
| Steralize Prior To Use | false |
| Device Is Sterile | true |
| Public Version Status | New |
| Device Record Status | Published |
| Public Version Number | 1 |
| Public Version Date | 2022-02-28 |
| Device Publish Date | 2022-02-18 |
| 10884450569341 | 00884450569344 |
| 10884450569266 | 00884450569269 |
| 20884450569317 | 00884450569313 |
| 10884450569297 | 00884450569290 |
| 20884450569720 | 00884450569726 |
| 10884450569334 | 00884450569337 |
| 20884450569256 | 00884450569252 |
| 10884450567323 | 00884450567326 |
| 20884450569287 | 00884450569283 |
| 10884450569778 | 00884450569771 |
| 20884450569355 | 00884450569351 |
| 20884450569300 | 00884450569306 |
| 10884450569365 | 00884450569368 |
| 20884450569379 | A |
| 20884450859593 | T |
| 20884450859609 | T |
| 10884450859671 | T |
| 10884450859657 | T |
| 10884450859619 | T |
| 20884450859586 | T |