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 |