| Primary Device ID | 00884450495087 |
| NIH Device Record Key | 9e1d9597-a04a-4b0d-a658-f3119ef2ea65 |
| Commercial Distribution Status | In Commercial Distribution |
| Brand Name | Hydrophilic Prelude SNAP™ |
| Version Model Number | 10884450495084 |
| Catalog Number | PLSH-1008/A |
| Company DUNS | 184763290 |
| Company Name | Merit Medical Systems, Inc. |
| Device Count | 5 |
| 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 Issuing Agency | Device ID |
|---|---|
| GS1 | 00884450495087 [Unit of Use] |
| GS1 | 10884450495084 [Primary] |
| DYB | INTRODUCER, CATHETER |
| Steralize Prior To Use | false |
| Device Is Sterile | true |
| Public Version Status | New |
| Device Record Status | Published |
| Public Version Number | 1 |
| Public Version Date | 2021-02-03 |
| Device Publish Date | 2021-01-26 |
| 00884450495056 | 10884450495053 |
| 00884450495049 | 10884450495046 |
| 00884450495100 | 10884450495107 |
| 00884450495087 | 10884450495084 |
| 00884450495445 | 10884450495442 |
| 00884450495476 | 10884450495473 |
| 00884450495469 | 10884450495466 |
| 00884450495490 | 10884450495497 |
| 00884450495506 | 10884450495503 |
| 00884450495452 | 10884450495459 |
| 00884450495513 | 10884450495510 |
| 00884450495520 | 10884450495527 |
| 00884450495551 | 10884450495558 |
| 00884450495544 | 10884450495541 |
| 00884450495537 | 10884450495534 |
| 00884450495483 | A |