| Primary Device ID | 00763000226008 |
| NIH Device Record Key | 90656884-e5d3-4c88-88a8-a84a39f88c30 |
| Commercial Distribution Status | In Commercial Distribution |
| Brand Name | Heli-FX™ EndoAnchor™ System |
| Version Model Number | HG-18-90-42 |
| Company DUNS | 006261481 |
| Company Name | MEDTRONIC, 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 | false |
| Donation Id Number | false |
| Contains Natural Rubber Latex | false |
| Labeled No Natural Rubber Latex | false |
| RX Perscription | false |
| OTC Over-The-Counter | false |
| Phone | +1(800)633-8766 |
| Corporate.UDI@medtronic.com |
| Length | 42 Millimeter |
| Special Storage Condition, Specify | Between 0 and 0 *Keep dry |
| Device Issuing Agency | Device ID |
|---|---|
| GS1 | 00763000226008 [Primary] |
| OTD | Endovascular suturing system |
| Steralize Prior To Use | false |
| Device Is Sterile | true |
| Public Version Status | Update |
| Device Record Status | Published |
| Public Version Number | 2 |
| Public Version Date | 2020-05-06 |
| Device Publish Date | 2019-06-29 |
| 00763000025298 | TAA GUIDE DEVICE 42 EIFU |
| 00763000025281 | TAA GUIDE DEVICE 32 EIFU |
| 00763000025274 | TAA GUIDE DEVICE 22 EIFU |
| 00763000025267 | AAA GUIDE DEVICE 28 EIFU |
| 00763000025250 | AAA GUIDE DEVICE 22 EIFU |
| 00763000006686 | ANCILLARY ENDOANCHOR CASSETTE US |
| 00763000006679 | TAA GUIDE DEVICE 42 EIFU |
| 00763000006662 | TAA GUIDE DEVICE 32 EIFU |
| 00763000006655 | TAA GUIDE DEVICE 22 EIFU |
| 00763000006648 | TAA APPLIER DEVICE US EIFU |
| 00763000006631 | AAA GUIDE DEVICE 28 EIFU |
| 00763000006624 | AAA GUIDE DEVICE 22 EIFU |
| 00763000006617 | AAA APPLIER DEVICE US EIFU |
| 00763000225971 | GUIDE HG-16-62-28 AAA ENDOANCH 28 EIFU |
| 00763000225964 | GUIDE SG-64 AAA ENDOANCHOR EIFU |
| 00763000226008 | GUIDE HG-18-90-42 TAA ENDOANCH 42 EIFU |
| 00763000225995 | GUIDE HG-18-90-32 TAA ENDOANCH 32 EIFU |
| 00763000225988 | GUIDE HG-18-90-22 TAA ENDOANCH 22 EIFU |
| 00763000225940 | ACC HA-18-114 TAA APPL-CASS 10 EIFU US |
| 00763000225933 | ACC SA-85 AAA APPL-CASSETTE 10 EIFU US |
| 00763000225957 | ACC EC-05 ANCIL ENDOANCHOR CASSETTE US |
| 00763000645120 | GUIDE SG-64 AAA ENDOANCHOR 22 EIFU US |
| 00763000645113 | ACC SA-85 AAA APPL-CASSETTE 10 EIFU US |
Mark Image Registration | Serial | Company Trademark Application Date |
|---|---|
![]() HELI-FX 85910990 not registered Dead/Abandoned |
Aptus Endosystems, Inc. 2013-04-22 |
![]() HELI-FX 85426860 4564541 Live/Registered |
MEDTRONIC VASCULAR, INC. 2011-09-20 |