GUDID 00887517102560

NV ET Tube, 6mm I.D. EMG

Nuvasive, Inc.

Neurophysiologic monitoring system

• Primary Device ID: 00887517102560
• NIH Device Record Key: ef171b73-f617-482f-99eb-5972ea55c885
• Commercial Distribution Status: In Commercial Distribution
• Version Model Number: 1552360
• Company DUNS: 053950783
• Company Name: Nuvasive, Inc.
• Device Count: 1
• DM Exempt: false
• Pre-market Exempt: false
• MRI Safety Status: Labeling does not contain MRI Safety Information
• Human Cell/Tissue Product: false
• Device Kit: false
• Device Combination Product: false
• Single Use: true
• Lot Batch: true
• Serial Number: false
• Manufacturing Date: false
• Expiration Date: false
• Donation Id Number: false
• Contains Natural Rubber Latex: false
• Labeled No Natural Rubber Latex: false
• RX Perscription: true
• OTC Over-The-Counter: false

Customer Support Contacts

• Phone: +1(858)909-1800
• Email: RA_UDI@nuvasive.com
• Phone: +1800-475-9131
• Email: nuvainfo@globusmedical.com
• Phone: +1800-475-9131
• Email: nuvainfo@globusmedical.com
• Phone: +1800-475-9131
• Email: nuvainfo@globusmedical.com
• Phone: +1800-475-9131
• Email: nuvainfo@globusmedical.com
• Phone: +1800-475-9131
• Email: nuvainfo@globusmedical.com
• Phone: +1800-475-9131
• Email: nuvainfo@globusmedical.com
• Phone: +1800-475-9131
• Email: nuvainfo@globusmedical.com
• Phone: +1800-475-9131
• Email: nuvainfo@globusmedical.com
• Phone: +1800-475-9131
• Email: nuvainfo@globusmedical.com
• Phone: +1800-475-9131
• Email: nuvainfo@globusmedical.com
• Phone: +1800-475-9131
• Email: nuvainfo@globusmedical.com
• Phone: +1800-475-9131
• Email: nuvainfo@globusmedical.com
• Phone: +1800-475-9131
• Email: nuvainfo@globusmedical.com
• Phone: +1800-475-9131
• Email: nuvainfo@globusmedical.com
• Phone: +1800-475-9131
• Email: nuvainfo@globusmedical.com

Device Identifiers

Device Issuing Agency	Device ID
GS1	00887517102560 [Primary]

FDA Pre-market Approvals/Notifications & deNovo

• Premarket Notification: K133530

FDA Product Code

• BSK: Cuff, tracheal tube, inflatable

Sterilization

• Steralize Prior To Use: true
• Device Is Sterile: false

[00887517102560]

Moist Heat or Steam Sterilization

[00887517102560]

Moist Heat or Steam Sterilization

[00887517102560]

Moist Heat or Steam Sterilization

[00887517102560]

Moist Heat or Steam Sterilization

[00887517102560]

Moist Heat or Steam Sterilization

[00887517102560]

Moist Heat or Steam Sterilization

[00887517102560]

Moist Heat or Steam Sterilization

[00887517102560]

Moist Heat or Steam Sterilization

[00887517102560]

Moist Heat or Steam Sterilization

[00887517102560]

Moist Heat or Steam Sterilization

[00887517102560]

Moist Heat or Steam Sterilization

[00887517102560]

Moist Heat or Steam Sterilization

[00887517102560]

Moist Heat or Steam Sterilization

[00887517102560]

Moist Heat or Steam Sterilization

[00887517102560]

Moist Heat or Steam Sterilization

[00887517102560]

Moist Heat or Steam Sterilization

Device Entry Metadata

• Public Version Status: New
• Device Record Status: Published
• Public Version Number: 1
• Public Version Date: 2019-07-23
• Device Publish Date: 2019-07-15

Devices Manufactured by Nuvasive, Inc.

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• 00195377147592 - ReLine: 2025-08-11 RELINE-ONE Shankdriver, Cam Lock
• 00195377148209 - ReLine: 2025-08-11 RELINE-ONE Shankdriver, w/o Blade Atch
• 00195377148216 - ReLine: 2025-08-11 RELINE-ONE Handle, Ratchet Retraction
• 00195377148223 - ReLine: 2025-08-11 RELINE-ONE Instrument Tray, Handle
• 00195377148261 - ReLine: 2025-08-11 RELINE-ONE Vector, 20mm Fluoro
• 00195377148278 - ReLine: 2025-08-11 RELINE-ONE Vector, 25mm Fluoro
• 00195377148285 - ReLine: 2025-08-11 RELINE-ONE Vector, 30mm Fluoro