Triad

GUDID 00887517265807

Triad Cervical Trial, 8x14x11mm Lord

Nuvasive, Inc.

Spinal implant trial

• Primary Device ID: 00887517265807
• NIH Device Record Key: 67c224a2-6a82-4655-aa47-80a9c22635dd
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: Triad
• Version Model Number: 5788114
• Company DUNS: 053950783
• Company Name: Nuvasive, Inc.
• Device Count: 1
• DM Exempt: false
• Pre-market Exempt: true
• 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: +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	00887517265807 [Primary]

FDA Product Code

• LXH: ORTHOPEDIC MANUAL SURGICAL INSTRUMENT

Sterilization

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

[00887517265807]

Moist Heat or Steam Sterilization

[00887517265807]

Moist Heat or Steam Sterilization

[00887517265807]

Moist Heat or Steam Sterilization

[00887517265807]

Moist Heat or Steam Sterilization

[00887517265807]

Moist Heat or Steam Sterilization

[00887517265807]

Moist Heat or Steam Sterilization

[00887517265807]

Moist Heat or Steam Sterilization

[00887517265807]

Moist Heat or Steam Sterilization

[00887517265807]

Moist Heat or Steam Sterilization

[00887517265807]

Moist Heat or Steam Sterilization

[00887517265807]

Moist Heat or Steam Sterilization

[00887517265807]

Moist Heat or Steam Sterilization

[00887517265807]

Moist Heat or Steam Sterilization

[00887517265807]

Moist Heat or Steam Sterilization

[00887517265807]

Moist Heat or Steam Sterilization

[00887517265807]

Moist Heat or Steam Sterilization

[00887517265807]

Moist Heat or Steam Sterilization

Device Entry Metadata

• Public Version Status: Update
• Device Record Status: Published
• Public Version Number: 2
• Public Version Date: 2019-02-07
• Device Publish Date: 2018-09-17

On-Brand Devices [Triad]

• 00887517525123: Triad ALIF Allograft Instruments
• 00887517518187: Cervical Rasp Set
• 00887517517609: Cervical Ins Set
• 00887517515902: Alpha Triad ALIF Allo Large Instruments
• 00887517265814: Triad Cervical Trial, 9x14x11mm Lord
• 00887517265807: Triad Cervical Trial, 8x14x11mm Lord
• 00887517265494: Triad Cervical Trial, 7x14x11mm Lord
• 00887517265487: Triad Cervical Trial, 6x14x11mm Lord
• 00887517265456: Triad Cervical Trial, 11x14x11mm Lord
• 00887517265449: Triad Cervical Trial, 10x14x11mm Lord
• 00887517265432: Triad Cervical Rasp, 12x14x11mm Lord
• 00887517265425: Triad Cervical Rasp, 11x14x11mm Lord
• 00887517265418: Triad Cervical Rasp, 10x14x11mm Lord
• 00887517265401: Triad Cervical Rasp, 9x14x11mm Lord
• 00887517265098: Triad Cervical Rasp, 8x14x11mm Lord
• 00887517265081: Triad Cervical Rasp, 7x14x11mm Lord
• 00887517265074: Triad Cervical Rasp, 6x14x11mm Lord
• 00887517265067: Triad Cervical Rasp, 5x14x11mm Lord
• 00887517265050: Triad Cervical Rasp, 12x11x11mm
• 00887517265043: Triad Cervical Rasp, 11x11x11mm
• 00887517265036: Triad Cervical Rasp, 10x11x11mm
• 00887517265029: Triad Cervical Rasp, 9x11x11mm
• 00887517265012: Triad Cervical Rasp, 8x11x11mm
• 00887517265005: Triad Cervical Rasp, 7x11x11mm
• 00887517264787: Triad Cervical Rasp, 5x11x11mm
• 00887517264770: Triad Cervical Rasp, 4x11x11mm
• 00887517264763: Triad Cervical Trial,9x14x11mm
• 00887517264749: Triad Cervical Trial, 8x14x11mm
• 00887517264725: Triad Cervical Trial, 7x14x11mm
• 00887517264701: Triad Cervical Trial, 6x14x11mm
• 00887517264282: Triad Cervical Trial, 5x14x11mm
• 00887517263773: Triad Cervical Inserter, Interbody Short
• 00887517263759: Triad Cervical Trial, 11x11x14mm
• 00887517261427: Triad Cervical Trial, 8mm 7°
• 00887517212375: Triad ALIF Allograft Tamp
• 00887517212368: Triad ALIF Tamp, Single Chamber
• 00887517144560: Triad ALIF Tamp, 38mm
• 00887517112040: Triad ALIF Tamp, 42mm Dual Chamber
• 00887517112033: Triad ALIF Tamp, 38mm Dual Chamber
• 00887517112026: Triad ALIF Tamp, 34mm Dual Chamber
• 00887517089533: Triad ALIF Tamp, 42mm
• 00887517075734: Triad ALIF Tamp, 34mm
• 00887517067890: 14mm Paddle Distractor Assy
• 00887517067883: 12mm Paddle Distractor Assy Color Coded
• 00887517067876: 10mm Paddle Distractor Assy Color Coded
• 00887517067869: 8mm Paddle Distractor Assy Color Coded
• 00887517067845: 14mm Paddle Distractor Assembly
• 00887517067838: 13mm Paddle Distractor Assembly
• 00887517067821: 12mm Paddle Distractor Assembly
• 00887517067814: 11mm Paddle Distractor Assembly