GUDID 20613994910794

LEAD WIRE DSE0004 10PK 1.2M GRN EXT ROHS

MEDTRONIC XOMED, INC.

Transcutaneous electrical stimulation lead
Primary Device ID20613994910794
NIH Device Record Key935cb7a9-8f17-4c19-af95-a1b4aae2e76a
Commercial Distribution StatusIn Commercial Distribution
Version Model NumberDSE0004
Company DUNS835465063
Company NameMEDTRONIC XOMED, INC.
Device Count1
DM Exemptfalse
Pre-market Exemptfalse
MRI Safety StatusLabeling does not contain MRI Safety Information
Human Cell/Tissue Productfalse
Device Kitfalse
Device Combination Productfalse
Single Usefalse
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
GS100613994910790 [Primary]
GS120613994910794 [Package]
Contains: 00613994910790
Package: PK [10 Units]
In Commercial Distribution

FDA Pre-market Approvals/Notifications & deNovo

FDA Product Code

GWJSTIMULATOR, AUDITORY, EVOKED RESPONSE

Sterilization

Steralize Prior To Usefalse
Device Is Sterilefalse

Device Entry Metadata

Public Version StatusUpdate
Device Record StatusPublished
Public Version Number3
Public Version Date2018-07-06
Device Publish Date2016-04-30

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