GUDID 20613994330073

WIRE 945DSE0005 1.2M48IN ASSORTED LEAD

MEDTRONIC XOMED, INC.

Subdermal needle electrode
Primary Device ID20613994330073
NIH Device Record Key8f3ea97b-8e6e-40e7-8e5f-ffa744504a71
Commercial Distribution StatusIn Commercial Distribution
Version Model Number945DSE0005
Company DUNS835465063
Company NameMEDTRONIC XOMED, 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 Batchtrue
Serial Numberfalse
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

Device Dimensions

Length1.2 Meter
Length1.2 Meter

Device Identifiers

Device Issuing AgencyDevice ID
GS100613994330079 [Primary]
GS120613994330073 [Package]
Contains: 00613994330079
Package: PK [10 Units]
In Commercial Distribution

FDA Pre-market Approvals/Notifications & deNovo

FDA Product Code

GWFSTIMULATOR, ELECTRICAL, EVOKED RESPONSE

Sterilization

Steralize Prior To Usefalse
Device Is Steriletrue

Device Entry Metadata

Public Version StatusUpdate
Device Record StatusPublished
Public Version Number3
Public Version Date2018-07-06
Device Publish Date2016-10-08

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