| Primary Device ID | 00763000006617 | 
| NIH Device Record Key | dd9c665d-d84b-4a9f-b8c4-022a6b43e113 | 
| Commercial Distribution Status | In Commercial Distribution | 
| Brand Name | Heli-FX™ EndoAnchor™ System | 
| Version Model Number | SA-85 | 
| Company DUNS | 006261481 | 
| Company Name | MEDTRONIC, INC. | 
| 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 | 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 | |
| Phone | +1(800)633-8766 | 
| Corporate.UDI@medtronic.com | 
| Length | 86 Centimeter | 
| Length | 86 Centimeter | 
| Special Storage Condition, Specify | Between 0 and 0 *Keep dry | 
| Special Storage Condition, Specify | Between 0 and 0 *Keep dry | 
| Device Issuing Agency | Device ID | 
|---|---|
| GS1 | 00763000006617 [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 | 6 | 
| Public Version Date | 2020-05-06 | 
| Device Publish Date | 2017-08-06 | 
| 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 |