Verify® External Neurostimulator

GUDID 00763000344573

ENS 353101 VERIFY ISTM US EMANUAL

MEDTRONIC, INC.

Sacral plexus percutaneous incontinence-control electrical stimulation system pulse generator Sacral plexus percutaneous incontinence-control electrical stimulation system pulse generator Sacral plexus percutaneous incontinence-control electrical stimulation system pulse generator Sacral plexus percutaneous incontinence-control electrical stimulation system pulse generator Sacral plexus percutaneous incontinence-control electrical stimulation system pulse generator Sacral plexus percutaneous incontinence-control electrical stimulation system pulse generator Sacral plexus percutaneous incontinence-control electrical stimulation system pulse generator Sacral plexus percutaneous incontinence-control electrical stimulation system pulse generator Sacral plexus percutaneous incontinence-control electrical stimulation system pulse generator Sacral plexus percutaneous incontinence-control electrical stimulation system pulse generator Sacral plexus percutaneous incontinence-control electrical stimulation system pulse generator Sacral plexus percutaneous incontinence-control electrical stimulation system pulse generator Sacral plexus percutaneous incontinence-control electrical stimulation system pulse generator Sacral plexus percutaneous incontinence-control electrical stimulation system pulse generator Sacral plexus percutaneous incontinence-control electrical stimulation system pulse generator
Primary Device ID00763000344573
NIH Device Record Key6beed998-6ff7-48ac-ab2b-6cc97c9e57c3
Commercial Distribution StatusIn Commercial Distribution
Brand NameVerify® External Neurostimulator
Version Model Number353101
Company DUNS796986144
Company NameMEDTRONIC, INC.
Device Count1
DM Exempttrue
Pre-market Exemptfalse
MRI Safety StatusLabeling does not contain MRI Safety Information
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

Device Identifiers

Device Issuing AgencyDevice ID
GS100763000344573 [Primary]

FDA Pre-market Approvals/Notifications & deNovo

FDA Product Code

EZWStimulator, electrical, implantable, for incontinence

Sterilization

Steralize Prior To Usefalse
Device Is Sterilefalse

Device Entry Metadata

Public Version StatusNew
Device Record StatusPublished
Public Version Number1
Public Version Date2020-10-05
Device Publish Date2020-09-25

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Trademark Results [Verify]

Mark Image

Registration | Serial
Company
Trademark
Application Date
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FIZEN TECHNOLOGY, LLC
2024-04-13
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2023-10-12
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TEGNA Inc.
2022-06-10
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TEGNA Inc.
2022-06-10
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97361880 not registered Live/Pending
Zymo Research Corporation
2022-04-13
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88503872 not registered Live/Pending
Novartis AG
2019-07-08
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88466703 5948788 Live/Registered
SMD SOLUTION Co., Ltd.
2019-06-10
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88124406 not registered Live/Pending
SMD SOLUTION Co., Ltd.
2018-09-20
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88124403 not registered Live/Pending
SMD SOLUTION Co., Ltd.
2018-09-20
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87975746 5428571 Live/Registered
The Retail Equation, Inc.
2017-04-04
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