GUDID 08714729760559

35cm 8 Contact Extension Kit

BOSTON SCIENTIFIC NEUROMODULATION CORPORATION

Spinal cord/peripheral nerve implantable analgesic electrical stimulation system lead extension Spinal cord/peripheral nerve implantable analgesic electrical stimulation system lead extension Spinal cord/peripheral nerve implantable analgesic electrical stimulation system lead extension Spinal cord/peripheral nerve implantable analgesic electrical stimulation system lead extension Spinal cord/peripheral nerve implantable analgesic electrical stimulation system lead extension Spinal cord/peripheral nerve implantable analgesic electrical stimulation system lead extension Spinal cord/peripheral nerve implantable analgesic electrical stimulation system lead extension Spinal cord/peripheral nerve implantable analgesic electrical stimulation system lead extension Spinal cord/peripheral nerve implantable analgesic electrical stimulation system lead extension Spinal cord/peripheral nerve implantable analgesic electrical stimulation system lead extension Spinal cord/peripheral nerve implantable analgesic electrical stimulation system lead extension Spinal cord/peripheral nerve implantable analgesic electrical stimulation system lead extension Spinal cord/peripheral nerve implantable analgesic electrical stimulation system lead extension Spinal cord/peripheral nerve implantable analgesic electrical stimulation system lead extension Spinal cord/peripheral nerve implantable analgesic electrical stimulation system lead extension Spinal cord/peripheral nerve implantable analgesic electrical stimulation system lead extension Spinal cord/peripheral nerve implantable analgesic electrical stimulation system lead extension
Primary Device ID08714729760559
NIH Device Record Key254a23a0-2635-4118-aa3f-c7df88942a08
Commercial Distribution StatusIn Commercial Distribution
Version Model NumberSC-3138-35
Company DUNS824951958
Company NameBOSTON SCIENTIFIC NEUROMODULATION CORPORATION
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 Numbertrue
Manufacturing Datefalse
Expiration Datetrue
Donation Id Numberfalse
Contains Natural Rubber Latexfalse
Labeled No Natural Rubber Latexfalse
RX Perscriptiontrue
OTC Over-The-Counterfalse

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Device Identifiers

Device Issuing AgencyDevice ID
GS108714729760559 [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 StatusUpdate
Device Record StatusPublished
Public Version Number4
Public Version Date2024-03-19
Device Publish Date2015-12-14

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