ILIF

GUDID 00887517263322

ILIF Inserter, Tanged

Nuvasive, Inc.

Orthopaedic implant inserter/extractor, reusable

• Primary Device ID: 00887517263322
• NIH Device Record Key: 9ce29147-7a3f-4d6b-ac29-bb99d3762729
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: ILIF
• Version Model Number: 5760140
• 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: +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

Device Identifiers

Device Issuing Agency	Device ID
GS1	00887517263322 [Primary]

FDA Product Code

• LXH: ORTHOPEDIC MANUAL SURGICAL INSTRUMENT

Sterilization

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

[00887517263322]

Moist Heat or Steam Sterilization

[00887517263322]

Moist Heat or Steam Sterilization

[00887517263322]

Moist Heat or Steam Sterilization

[00887517263322]

Moist Heat or Steam Sterilization

[00887517263322]

Moist Heat or Steam Sterilization

[00887517263322]

Moist Heat or Steam Sterilization

[00887517263322]

Moist Heat or Steam Sterilization

[00887517263322]

Moist Heat or Steam Sterilization

[00887517263322]

Moist Heat or Steam Sterilization

[00887517263322]

Moist Heat or Steam Sterilization

[00887517263322]

Moist Heat or Steam Sterilization

[00887517263322]

Moist Heat or Steam Sterilization

[00887517263322]

Moist Heat or Steam Sterilization

Device Entry Metadata

• Public Version Status: Update
• Device Record Status: Published
• Public Version Number: 4
• Public Version Date: 2019-04-23
• Device Publish Date: 2018-09-24

On-Brand Devices [ILIF]

• 00887517519153: Interspinous General Ins Set
• 00887517515513: Alpha H3 Trial Tray
• 00887517263711: ILIF Trial, 20mm
• 00887517263704: ILIF Trial, 18mm
• 00887517263391: ILIF Trial, 16mm
• 00887517263384: ILIF Trial, 14mm
• 00887517263377: ILIF Trial, 12mm
• 00887517263360: ILIF Trial, 10mm
• 00887517263353: ILIF Trial, 8mm
• 00887517263339: ILIF Tamp
• 00887517263322: ILIF Inserter, Tanged
• 00887517262899: ILIF Rack Distractor
• 00887517262882: ILIF Shovel Tip, Long
• 00887517262868: ILIF Distractor Tube
• 00887517262851: ILIF Shovel Tip
• 00887517262837: ILIF Driver, Caspar Pin
• 00887517257529: ILIF Rasp
• 00887517257192: ILIF Tissue Dissector
• 00887517984920: RMM Navigation.S Instruments
• 00887517709493: MAS Midline Trial, L
• 00887517709486: MAS Midline Trial, M
• 00887517709479: MAS Midline Trial, S
• 00887517262813: Tray - Interspinous Instruments (Base)