| Primary Device ID | 00888707007634 |
| NIH Device Record Key | 3a413f07-72ce-46a3-8125-0916bb4b77fc |
| Commercial Distribution Status | In Commercial Distribution |
| Brand Name | HVAD® Pump Outflow Graft |
| Version Model Number | MCS1725OG |
| Catalog Number | MCS1725OG |
| Company DUNS | 146054536 |
| Company Name | Heartware 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 | false |
| Serial Number | true |
| Manufacturing Date | true |
| Expiration Date | true |
| Donation Id Number | false |
| Contains Natural Rubber Latex | false |
| Labeled No Natural Rubber Latex | true |
| RX Perscription | true |
| OTC Over-The-Counter | false |
| Device Issuing Agency | Device ID |
|---|---|
| GS1 | 00888707007634 [Primary] |
| DSQ | Ventricular (Assist) Bypass |
| Steralize Prior To Use | false |
| Device Is Sterile | true |
| Public Version Status | New |
| Device Record Status | Published |
| Public Version Number | 1 |
| Public Version Date | 2020-12-22 |
| Device Publish Date | 2020-12-14 |
| 00888707000222 | 1125 |
| 00888707007634 | MCS1725OG |
| 00888707007641 | 1125 |
Mark Image Registration | Serial | Company Trademark Application Date |
|---|---|
![]() HVAD 85758552 not registered Dead/Abandoned |
HeartWare Inc. 2012-10-19 |
![]() HVAD 78910214 3730135 Live/Registered |
HeartWare, Inc. 2006-06-16 |