Intellis™ Pro

GUDID 00763000558826

INS 977118 INTELLIS PRO US EMAN

MEDTRONIC, INC.

Spinal cord/peripheral nerve implantable analgesic electrical stimulation system pulse generator, implantable Spinal cord/peripheral nerve implantable analgesic electrical stimulation system pulse generator, implantable Spinal cord/peripheral nerve implantable analgesic electrical stimulation system pulse generator, implantable Spinal cord/peripheral nerve implantable analgesic electrical stimulation system pulse generator, implantable Spinal cord/peripheral nerve implantable analgesic electrical stimulation system pulse generator, implantable Spinal cord/peripheral nerve implantable analgesic electrical stimulation system pulse generator, implantable Spinal cord/peripheral nerve implantable analgesic electrical stimulation system pulse generator, implantable Spinal cord/peripheral nerve implantable analgesic electrical stimulation system pulse generator, implantable Spinal cord/peripheral nerve implantable analgesic electrical stimulation system pulse generator, implantable Spinal cord/peripheral nerve implantable analgesic electrical stimulation system pulse generator, implantable Spinal cord/peripheral nerve implantable analgesic electrical stimulation system pulse generator, implantable Spinal cord/peripheral nerve implantable analgesic electrical stimulation system pulse generator, implantable Spinal cord/peripheral nerve implantable analgesic electrical stimulation system pulse generator, implantable Spinal cord/peripheral nerve implantable analgesic electrical stimulation system pulse generator, implantable Spinal cord/peripheral nerve implantable analgesic electrical stimulation system pulse generator, implantable Spinal cord/peripheral nerve implantable analgesic electrical stimulation system pulse generator, implantable Spinal cord/peripheral nerve implantable analgesic electrical stimulation system pulse generator, implantable
Primary Device ID00763000558826
NIH Device Record Key9968ec89-31cb-4fc1-a14a-3ee6a599823f
Commercial Distribution StatusIn Commercial Distribution
Brand NameIntellis™ Pro
Version Model Number977118
Company DUNS796986144
Company NameMEDTRONIC, INC.
Device Count1
DM Exemptfalse
Pre-market Exemptfalse
MRI Safety StatusMR Conditional
Human Cell/Tissue Productfalse
Device Kitfalse
Device Combination Productfalse
Single Usetrue
Lot Batchfalse
Serial Numbertrue
Manufacturing Datefalse
Expiration Datefalse
Donation Id Numberfalse
Contains Natural Rubber Latexfalse
Labeled No Natural Rubber Latexfalse
RX Perscriptiontrue
OTC Over-The-Counterfalse

Customer Support Contacts

Phone+1(800)633-8766
EmailCorporate.UDI@medtronic.com
Phone+1(800)633-8766
EmailCorporate.UDI@medtronic.com
Phone+1(800)633-8766
EmailCorporate.UDI@medtronic.com
Phone+1(800)633-8766
EmailCorporate.UDI@medtronic.com
Phone+1(800)633-8766
EmailCorporate.UDI@medtronic.com
Phone+1(800)633-8766
EmailCorporate.UDI@medtronic.com
Phone+1(800)633-8766
EmailCorporate.UDI@medtronic.com
Phone+1(800)633-8766
EmailCorporate.UDI@medtronic.com
Phone+1(800)633-8766
EmailCorporate.UDI@medtronic.com
Phone+1(800)633-8766
EmailCorporate.UDI@medtronic.com
Phone+1(800)633-8766
EmailCorporate.UDI@medtronic.com
Phone+1(800)633-8766
EmailCorporate.UDI@medtronic.com
Phone+1(800)633-8766
EmailCorporate.UDI@medtronic.com
Phone+1(800)633-8766
EmailCorporate.UDI@medtronic.com
Phone+1(800)633-8766
EmailCorporate.UDI@medtronic.com
Phone+1(800)633-8766
EmailCorporate.UDI@medtronic.com
Phone+1(800)633-8766
EmailCorporate.UDI@medtronic.com

Device Identifiers

Device Issuing AgencyDevice ID
GS100763000558826 [Primary]

FDA Pre-market Approvals/Notifications & deNovo

FDA Product Code

LGWStimulator, spinal-cord, totally implanted for pain relief

Sterilization

Steralize Prior To Usefalse
Device Is Steriletrue

Device Entry Metadata

Public Version StatusNew
Device Record StatusPublished
Public Version Number1
Public Version Date2024-05-13
Device Publish Date2024-05-05

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00763000902568 - Launcher™2024-06-04 CATHETER LA83DRIGHT LA 8F 100CM 3DRGT
00763000902575 - Launcher™2024-06-04 CATHETER LA83DRIGHTD LA 8F 90CM 3DRGT
00763000902582 - Launcher™2024-06-04 CATHETER LA8AL10 LA 8F 100CM AL10
00763000902599 - Launcher™2024-06-04 CATHETER LA8AL10D LA 8F 90CM AL10
00763000902605 - Launcher™2024-06-04 CATHETER LA8AL10F LA 8F 80CM AL10

Trademark Results [Intellis]

Mark Image

Registration | Serial
Company
Trademark
Application Date
INTELLIS
INTELLIS
90006780 not registered Live/Pending
EASTECH FLOW CONTROLS, INC.
2020-06-17
INTELLIS
INTELLIS
88466477 not registered Live/Pending
Anark Corporation
2019-06-10
INTELLIS
INTELLIS
87537382 5466297 Live/Registered
Medtronic, Inc.
2017-07-21
INTELLIS
INTELLIS
87476725 not registered Dead/Abandoned
Warshaw Group, Inc.
2017-06-06
INTELLIS
INTELLIS
86217882 not registered Dead/Abandoned
Medtronic, Inc.
2014-03-11
INTELLIS
INTELLIS
85128349 not registered Dead/Abandoned
Medtronic, Inc.
2010-09-13
INTELLIS
INTELLIS
77368977 3637443 Live/Registered
WESTLOCK CONTROLS CORPORATION
2008-01-10
INTELLIS
INTELLIS
76214003 2847960 Dead/Cancelled
BLACKROCK INSTITUTIONAL TRUST COMPANY, NATIONAL ASSOCIATION
2001-02-21
INTELLIS
INTELLIS
73601689 1421791 Dead/Cancelled
SCHLAGE LOCK COMPANY
1986-06-02
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