GUDID 00643169157774

LEAD 3875-45 OCTAD 1X8 BNT STYLT EMAN US

MEDTRONIC, INC.

Analgesic spinal cord electrical stimulation system
Primary Device ID00643169157774
NIH Device Record Keybd3799a0-a483-471e-b0b9-1825cd99dfba
Commercial Distribution StatusIn Commercial Distribution
Version Model Number3875-45
Company DUNS796986144
Company NameMEDTRONIC, 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 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
Phone+1(800)633-8766
EmailCorporate.UDI@medtronic.com

Device Dimensions

Length45 Centimeter
Length45 Centimeter
Length45 Centimeter

Device Identifiers

Device Issuing AgencyDevice ID
GS100643169157774 [Primary]

FDA Pre-market Approvals/Notifications & deNovo

FDA Product Code

GZBSTIMULATOR, SPINAL-CORD, IMPLANTED (PAIN RELIEF)

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 Date2015-06-08

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