| Primary Device ID | 08714729808091 |
| NIH Device Record Key | dca5be3b-7431-4097-8eb7-fb32110125aa |
| Commercial Distribution Status | In Commercial Distribution |
| Brand Name | PROMUS Element™ Plus |
| Version Model Number | H7493911424400 |
| Catalog Number | H7493911424400 |
| Company DUNS | 021717889 |
| Company Name | BOSTON SCIENTIFIC CORPORATION |
| Device Count | 1 |
| DM Exempt | false |
| Pre-market Exempt | false |
| MRI Safety Status | MR Conditional |
| Human Cell/Tissue Product | false |
| Device Kit | false |
| Device Combination Product | true |
| 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 | true |
| 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 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 | 08714729808091 [Primary] |
| NIQ | Coronary drug-eluting stent |
| Steralize Prior To Use | false |
| Device Is Sterile | true |
| Public Version Status | Update |
| Device Record Status | Published |
| Public Version Number | 4 |
| Public Version Date | 2019-10-07 |
| Device Publish Date | 2014-09-24 |
| 08714729807742 | Everolimus-Eluting Platinum Chromium Coronary Stent System |
| 08714729807735 | Everolimus-Eluting Platinum Chromium Coronary Stent System |
| 08714729807728 | Everolimus-Eluting Platinum Chromium Coronary Stent System |
| 08714729807704 | Everolimus-Eluting Platinum Chromium Coronary Stent System |
| 08714729807698 | Everolimus-Eluting Platinum Chromium Coronary Stent System |
| 08714729807681 | Everolimus-Eluting Platinum Chromium Coronary Stent System |
| 08714729807650 | Everolimus-Eluting Platinum Chromium Coronary Stent System |
| 08714729807636 | Everolimus-Eluting Platinum Chromium Coronary Stent System |
| 08714729807629 | Everolimus-Eluting Platinum Chromium Coronary Stent System |
| 08714729807605 | Everolimus-Eluting Platinum Chromium Coronary Stent System |
| 08714729807599 | Everolimus-Eluting Platinum Chromium Coronary Stent System |
| 08714729807568 | Everolimus-Eluting Platinum Chromium Coronary Stent System |
| 08714729807551 | Everolimus-Eluting Platinum Chromium Coronary Stent System |
| 08714729807544 | Everolimus-Eluting Platinum Chromium Coronary Stent System |
| 08714729807537 | Everolimus-Eluting Platinum Chromium Coronary Stent System |
| 08714729807520 | Everolimus-Eluting Platinum Chromium Coronary Stent System |
| 08714729807513 | Everolimus-Eluting Platinum Chromium Coronary Stent System |
| 08714729807506 | Everolimus-Eluting Platinum Chromium Coronary Stent System |
| 08714729807476 | Everolimus-Eluting Platinum Chromium Coronary Stent System |
| 08714729807469 | Everolimus-Eluting Platinum Chromium Coronary Stent System |
| 08714729807452 | Everolimus-Eluting Platinum Chromium Coronary Stent System |
| 08714729807445 | Everolimus-Eluting Platinum Chromium Coronary Stent System |
| 08714729807438 | Everolimus-Eluting Platinum Chromium Coronary Stent System |
| 08714729807421 | Everolimus-Eluting Platinum Chromium Coronary Stent System |
| 08714729807414 | Everolimus-Eluting Platinum Chromium Coronary Stent System |
| 08714729807407 | Everolimus-Eluting Platinum Chromium Coronary Stent System |
| 08714729807391 | Everolimus-Eluting Platinum Chromium Coronary Stent System |
| 08714729807384 | Everolimus-Eluting Platinum Chromium Coronary Stent System |
| 08714729807360 | Everolimus-Eluting Platinum Chromium Coronary Stent System |
| 08714729807353 | Everolimus-Eluting Platinum Chromium Coronary Stent System |
| 08714729807346 | Everolimus-Eluting Platinum Chromium Coronary Stent System |
| 08714729807339 | Everolimus-Eluting Platinum Chromium Coronary Stent System |
| 08714729807322 | Everolimus-Eluting Platinum Chromium Coronary Stent System |
| 08714729807315 | Everolimus-Eluting Platinum Chromium Coronary Stent System |
| 08714729807308 | Everolimus-Eluting Platinum Chromium Coronary Stent System |
| 08714729807285 | Everolimus-Eluting Platinum Chromium Coronary Stent System |
| 08714729823773 | Everolimus-Eluting Platinum Chromium Coronary Stent System |
| 08714729823766 | Everolimus-Eluting Platinum Chromium Coronary Stent System |
| 08714729823759 | Everolimus-Eluting Platinum Chromium Coronary Stent System |
| 08714729823742 | Everolimus-Eluting Platinum Chromium Coronary Stent System |
| 08714729823735 | Everolimus-Eluting Platinum Chromium Coronary Stent System |
| 08714729823728 | Everolimus-Eluting Platinum Chromium Coronary Stent System |
| 08714729823711 | Everolimus-Eluting Platinum Chromium Coronary Stent System |
| 08714729823704 | Everolimus-Eluting Platinum Chromium Coronary Stent System |
| 08714729823698 | Everolimus-Eluting Platinum Chromium Coronary Stent System |
| 08714729823681 | Everolimus-Eluting Platinum Chromium Coronary Stent System |
| 08714729808114 | Everolimus-Eluting Platinum Chromium Coronary Stent System |
| 08714729808107 | Everolimus-Eluting Platinum Chromium Coronary Stent System |
| 08714729808091 | Everolimus-Eluting Platinum Chromium Coronary Stent System |
| 08714729808084 | Everolimus-Eluting Platinum Chromium Coronary Stent System |
Mark Image Registration | Serial | Company Trademark Application Date |
|---|---|
![]() PROMUS ELEMENT 78959893 3891512 Dead/Cancelled |
Boston Scientific Scimed, Inc. 2006-08-24 |