GUDID 00195377166029

Reline MAS Tap, Cannulated Detent, 7.0mm

Nuvasive, Inc.

Internal spinal fixation procedure kit, reusable

• Primary Device ID: 00195377166029
• NIH Device Record Key: 7292653d-26f7-417d-b303-c9a817795376
• Commercial Distribution Status: In Commercial Distribution
• Version Model Number: Z600471-070
• 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: false
• 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: +1(858)909-1800
• Email: RA_UDI@nuvasive.com
• Phone: +1(858)909-1800
• Email: RA_UDI@nuvasive.com
• Phone: +1(858)909-1800
• Email: RA_UDI@nuvasive.com
• Phone: +1(858)909-1800
• Email: RA_UDI@nuvasive.com
• Phone: +1(858)909-1800
• Email: RA_UDI@nuvasive.com
• Phone: +1(858)909-1800
• Email: RA_UDI@nuvasive.com
• Phone: +1(858)909-1800
• Email: RA_UDI@nuvasive.com
• Phone: +1(858)909-1800
• Email: RA_UDI@nuvasive.com
• Phone: +1(858)909-1800
• Email: RA_UDI@nuvasive.com
• Phone: +1(858)909-1800
• Email: RA_UDI@nuvasive.com
• Phone: +1(858)909-1800
• Email: RA_UDI@nuvasive.com
• Phone: +1(858)909-1800
• Email: RA_UDI@nuvasive.com
• Phone: +1(858)909-1800
• Email: RA_UDI@nuvasive.com
• Phone: +1(858)909-1800
• Email: RA_UDI@nuvasive.com
• Phone: +1(858)909-1800
• Email: nuvainfo@globusmedical.com
• Phone: +1(858)909-1800
• Email: nuvainfo@globusmedical.com
• Phone: +1(858)909-1800
• Email: nuvainfo@globusmedical.com
• Phone: +1(858)909-1800
• Email: nuvainfo@globusmedical.com
• Phone: +1(858)909-1800
• Email: nuvainfo@globusmedical.com
• Phone: +1(858)909-1800
• Email: nuvainfo@globusmedical.com
• Phone: +1(858)909-1800
• Email: nuvainfo@globusmedical.com
• Phone: +1(858)909-1800
• Email: nuvainfo@globusmedical.com
• Phone: +1(858)909-1800
• Email: nuvainfo@globusmedical.com
• Phone: +1(858)909-1800
• Email: nuvainfo@globusmedical.com
• Phone: +1(858)909-1800
• Email: nuvainfo@globusmedical.com
• Phone: +1(858)909-1800
• Email: nuvainfo@globusmedical.com
• Phone: +1(858)909-1800
• Email: nuvainfo@globusmedical.com
• Phone: +1(858)909-1800
• Email: nuvainfo@globusmedical.com
• Phone: +1(858)909-1800
• 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
• Phone: +1800-475-9131
• Email: nuvainfo@globusmedical.com

Device Identifiers

Device Issuing Agency	Device ID
GS1	00195377166029 [Primary]

FDA Pre-market Approvals/Notifications & deNovo

• Premarket Notification: K112709

FDA Product Code

• ETN: STIMULATOR, NERVE

Sterilization

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

[00195377166029]

Moist Heat or Steam Sterilization

[00195377166029]

Moist Heat or Steam Sterilization

[00195377166029]

Moist Heat or Steam Sterilization

[00195377166029]

Moist Heat or Steam Sterilization

[00195377166029]

Moist Heat or Steam Sterilization

[00195377166029]

Moist Heat or Steam Sterilization

[00195377166029]

Moist Heat or Steam Sterilization

[00195377166029]

Moist Heat or Steam Sterilization

[00195377166029]

Moist Heat or Steam Sterilization

[00195377166029]

Moist Heat or Steam Sterilization

[00195377166029]

Moist Heat or Steam Sterilization

[00195377166029]

Moist Heat or Steam Sterilization

[00195377166029]

Moist Heat or Steam Sterilization

[00195377166029]

Moist Heat or Steam Sterilization

[00195377166029]

Moist Heat or Steam Sterilization

[00195377166029]

Moist Heat or Steam Sterilization

[00195377166029]

Moist Heat or Steam Sterilization

[00195377166029]

Moist Heat or Steam Sterilization

[00195377166029]

Moist Heat or Steam Sterilization

[00195377166029]

Moist Heat or Steam Sterilization

[00195377166029]

Moist Heat or Steam Sterilization

[00195377166029]

Moist Heat or Steam Sterilization

[00195377166029]

Moist Heat or Steam Sterilization

[00195377166029]

Moist Heat or Steam Sterilization

[00195377166029]

Moist Heat or Steam Sterilization

[00195377166029]

Moist Heat or Steam Sterilization

[00195377166029]

Moist Heat or Steam Sterilization

[00195377166029]

Moist Heat or Steam Sterilization

[00195377166029]

Moist Heat or Steam Sterilization

[00195377166029]

Moist Heat or Steam Sterilization

[00195377166029]

Moist Heat or Steam Sterilization

[00195377166029]

Moist Heat or Steam Sterilization

[00195377166029]

Moist Heat or Steam Sterilization

[00195377166029]

Moist Heat or Steam Sterilization

[00195377166029]

Moist Heat or Steam Sterilization

[00195377166029]

Moist Heat or Steam Sterilization

[00195377166029]

Moist Heat or Steam Sterilization

[00195377166029]

Moist Heat or Steam Sterilization

[00195377166029]

Moist Heat or Steam Sterilization

[00195377166029]

Moist Heat or Steam Sterilization

[00195377166029]

Moist Heat or Steam Sterilization

[00195377166029]

Moist Heat or Steam Sterilization

[00195377166029]

Moist Heat or Steam Sterilization

[00195377166029]

Moist Heat or Steam Sterilization

Device Entry Metadata

• Public Version Status: New
• Device Record Status: Published
• Public Version Number: 1
• Public Version Date: 2024-01-15
• Device Publish Date: 2024-01-05

Devices Manufactured by Nuvasive, Inc.

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• 00887517017413 - Cohere: 2025-06-11 COHERE Pivoting Trial, 11x11x30mm 8°
• 00887517017420 - Cohere: 2025-06-11 COHERE Pivoting Trial, 11x11x34mm 8°
• 00887517017437 - Cohere: 2025-06-11 COHERE Pivoting Trial, 11x9x30mm 8°
• 00887517017444 - Cohere: 2025-06-11 COHERE Pivoting Trial, 12x11x30mm 15°
• 00887517017451 - Cohere: 2025-06-11 COHERE Pivoting Trial, 12x11x30mm 8°
• 00887517017468 - Cohere: 2025-06-11 COHERE Pivoting Trial, 12x11x34mm 8°
• 00887517017475 - Cohere: 2025-06-11 COHERE Pivoting Trial, 12x9x30mm 8°