Primary Device ID | 00763000849078 |
NIH Device Record Key | 4535df32-ee66-4ec2-8750-92823f60628f |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | Vanta™ AdaptiveStim™ |
Version Model Number | 977006 |
Company DUNS | 796986144 |
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 | false |
Serial Number | true |
Manufacturing Date | false |
Expiration Date | false |
Donation Id Number | false |
Contains Natural Rubber Latex | false |
Labeled No Natural Rubber Latex | false |
RX Perscription | true |
OTC Over-The-Counter | false |
Phone | +1(800)633-8766 |
Corporate.UDI@medtronic.com | |
Phone | +1(800)633-8766 |
Corporate.UDI@medtronic.com | |
Phone | +1(800)633-8766 |
Corporate.UDI@medtronic.com | |
Phone | +1(800)633-8766 |
Corporate.UDI@medtronic.com | |
Phone | +1(800)633-8766 |
Corporate.UDI@medtronic.com | |
Phone | +1(800)633-8766 |
Corporate.UDI@medtronic.com | |
Phone | +1(800)633-8766 |
Corporate.UDI@medtronic.com | |
Phone | +1(800)633-8766 |
Corporate.UDI@medtronic.com | |
Phone | +1(800)633-8766 |
Corporate.UDI@medtronic.com | |
Phone | +1(800)633-8766 |
Corporate.UDI@medtronic.com | |
Phone | +1(800)633-8766 |
Corporate.UDI@medtronic.com | |
Phone | +1(800)633-8766 |
Corporate.UDI@medtronic.com | |
Phone | +1(800)633-8766 |
Corporate.UDI@medtronic.com | |
Phone | +1(800)633-8766 |
Corporate.UDI@medtronic.com | |
Phone | +1(800)633-8766 |
Corporate.UDI@medtronic.com | |
Phone | +1(800)633-8766 |
Corporate.UDI@medtronic.com | |
Phone | +1(800)633-8766 |
Corporate.UDI@medtronic.com | |
Phone | +1(800)633-8766 |
Corporate.UDI@medtronic.com |
Device Issuing Agency | Device ID |
---|---|
GS1 | 00763000849078 [Primary] |
LGW | Stimulator, spinal-cord, totally implanted for pain relief |
Steralize Prior To Use | false |
Device Is Sterile | true |
Public Version Status | New |
Device Record Status | Published |
Public Version Number | 1 |
Public Version Date | 2024-05-27 |
Device Publish Date | 2024-05-19 |
20199150004151 - NA | 2025-04-07 CUSTOM PACK BB10V58R1 10PK SHELBY BPT PG |
20199150004311 - NA | 2025-04-07 CUSTOM PACK BB12P29R 4PK TABLE LNS |
00763000959616 - AEX | 2025-04-04 AEX GENERATOR 40-405-1R REFURB US |
20763000651736 - Aortic Punch | 2025-03-31 Aortic Punch APU425 - 2.5mm punch size |
20763000651743 - Aortic Punch | 2025-03-31 Aortic Punch APU430 - 3.0mm punch size |
20763000651750 - Aortic Punch | 2025-03-31 Aortic Punch APU435 - 3.5mm punch size |
20763000651767 - Aortic Punch | 2025-03-31 Aortic Punch APU440 - 4.0mm punch size |
20763000651774 - Aortic Punch | 2025-03-31 Aortic Punch APU444 - 4.4mm punch size |
Mark Image Registration | Serial | Company Trademark Application Date |
---|---|
VANTA 97891810 not registered Live/Pending |
Vanta Global, LLC 2023-04-17 |
VANTA 97830784 not registered Live/Pending |
Vanta Inc. 2023-03-09 |
VANTA 90144752 not registered Live/Pending |
Vanta Inc. 2020-08-28 |
VANTA 90144728 not registered Live/Pending |
Vanta Inc. 2020-08-28 |
VANTA 90072563 not registered Live/Pending |
Wilbur-Ellis Company LLC 2020-07-24 |
VANTA 88871429 not registered Live/Pending |
Vantage Group LLC 2020-04-14 |
VANTA 88681390 not registered Live/Pending |
Vanta Inc. 2019-11-05 |
VANTA 88420363 not registered Live/Pending |
Medtronic, Inc. 2019-05-08 |
VANTA 87717029 5534145 Live/Registered |
Olympus Corporation 2017-12-12 |
VANTA 87628820 5692806 Live/Registered |
VANTA EDUCATION, INC. 2017-09-29 |
VANTA 86749799 5080428 Live/Registered |
Olympus Corporation 2015-09-08 |
![]() VANTA 86200796 4851899 Live/Registered |
VANTA COMMERCIAL PROPERTIES L.L.C. 2014-02-21 |