GUDID 00887517159366

NVJJB Connector Adapter, Dual to DIN

Nuvasive, Inc.

Neurophysiologic monitoring system
Primary Device ID00887517159366
NIH Device Record Key26b50434-800c-4091-83a8-31b05ffae69e
Commercial Distribution StatusIn Commercial Distribution
Version Model Number2010017
Company DUNS053950783
Company NameNuvasive, 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(858)909-1800
EmailRA_UDI@nuvasive.com
Phone+1(858)909-1800
EmailRA_UDI@nuvasive.com
Phone+1(858)909-1800
EmailRA_UDI@nuvasive.com
Phone+1(858)909-1800
EmailRA_UDI@nuvasive.com
Phone+1(858)909-1800
EmailRA_UDI@nuvasive.com
Phone+1(858)909-1800
EmailRA_UDI@nuvasive.com
Phone+1(858)909-1800
EmailRA_UDI@nuvasive.com
Phone+1800-475-9131
Emailnuvainfo@globusmedical.com
Phone+1800-475-9131
Emailnuvainfo@globusmedical.com
Phone+1800-475-9131
Emailnuvainfo@globusmedical.com
Phone+1800-475-9131
Emailnuvainfo@globusmedical.com
Phone+1800-475-9131
Emailnuvainfo@globusmedical.com
Phone+1800-475-9131
Emailnuvainfo@globusmedical.com
Phone+1800-475-9131
Emailnuvainfo@globusmedical.com
Phone+1800-475-9131
Emailnuvainfo@globusmedical.com
Phone+1800-475-9131
Emailnuvainfo@globusmedical.com
Phone+1800-475-9131
Emailnuvainfo@globusmedical.com
Phone+1800-475-9131
Emailnuvainfo@globusmedical.com
Phone+1800-475-9131
Emailnuvainfo@globusmedical.com
Phone+1800-475-9131
Emailnuvainfo@globusmedical.com
Phone+1800-475-9131
Emailnuvainfo@globusmedical.com
Phone+1800-475-9131
Emailnuvainfo@globusmedical.com

Device Identifiers

Device Issuing AgencyDevice ID
GS100887517159366 [Primary]

FDA Pre-market Approvals/Notifications & deNovo

FDA Product Code

GWFStimulator, electrical, evoked response

Sterilization

Steralize Prior To Usefalse
Device Is Sterilefalse

Device Entry Metadata

Public Version StatusNew
Device Record StatusPublished
Public Version Number1
Public Version Date2024-04-15
Device Publish Date2024-04-05

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00195377148216 - ReLine2025-08-11 RELINE-ONE Handle, Ratchet Retraction
00195377148223 - ReLine2025-08-11 RELINE-ONE Instrument Tray, Handle

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