| Primary Device ID | 10884450292775 |
| NIH Device Record Key | fa8e3fc3-a3bd-4160-a55d-8ef5b67305d1 |
| Commercial Distribution Status | In Commercial Distribution |
| Brand Name | PhD™ |
| Version Model Number | 00884450292778 |
| Catalog Number | MAP854 |
| 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 | 00884450292778 [Primary] |
| GS1 | 10884450292775 [Package] Contains: 00884450292778 Package: [20 Units] In Commercial Distribution |
| GS1 | 20884450292772 [Package] Package: [4 Units] In Commercial Distribution |
| OEQ | Angiography/angioplasty kit |
| Steralize Prior To Use | false |
| Device Is Sterile | true |
| Public Version Status | New |
| Device Record Status | Published |
| Public Version Number | 1 |
| Public Version Date | 2020-09-01 |
| Device Publish Date | 2020-08-24 |
| 10884450160487 | 00884450160480 |
| 20884450160507 | 00884450160503 |
| 10884450292751 | 00884450292754 |
| 20884450160491 | 00884450160497 |
| 10884450160517 | 00884450160510 |
| 20884450292789 | 00884450292785 |
| 10884450291969 | 00884450291962 |
| 10884450160524 | 00884450160527 |
| 10884450292775 | 00884450292778 |
| 20884450746725 | 00884450746721 |
| 10884450746742 | 00884450746745 |
| 10884450746827 | 00884450746820 |
| 20884450746718 | 00884450746714 |
| 10884450746766 | 00884450746769 |
| 20884450746817 | 00884450746813 |
| 10884450746780 | B |