Axis Spine Technologies ALIF System Instrument 2984 00 210

GUDID 05056619800390

Sterilisation Case - Inner Layer (1 of 2)

AXIS SPINE TECHNOLOGIES LTD

Device sterilization/disinfection container, reusable

• Primary Device ID: 05056619800390
• NIH Device Record Key: 64d65767-8511-4f72-8f92-4d0565ad175a
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: Axis Spine Technologies ALIF System Instrument
• Version Model Number: 2984 00 210
• Catalog Number: 2984 00 210
• Company DUNS: 221947288
• Company Name: AXIS SPINE TECHNOLOGIES LTD
• 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: +443301230535
• Email: enquiries@axisspinetech.com
• Phone: +443301230535
• Email: enquiries@axisspinetech.com
• Phone: +443301230535
• Email: enquiries@axisspinetech.com
• Phone: +443301230535
• Email: enquiries@axisspinetech.com
• Phone: +443301230535
• Email: enquiries@axisspinetech.com
• Phone: +443301230535
• Email: enquiries@axisspinetech.com
• Phone: +443301230535
• Email: enquiries@axisspinetech.com
• Phone: +443301230535
• Email: enquiries@axisspinetech.com
• Phone: +443301230535
• Email: enquiries@axisspinetech.com
• Phone: +443301230535
• Email: enquiries@axisspinetech.com
• Phone: +443301230535
• Email: enquiries@axisspinetech.com
• Phone: +443301230535
• Email: enquiries@axisspinetech.com
• Phone: +443301230535
• Email: enquiries@axisspinetech.com
• Phone: +443301230535
• Email: enquiries@axisspinetech.com
• Phone: +443301230535
• Email: enquiries@axisspinetech.com
• Phone: +443301230535
• Email: enquiries@axisspinetech.com

Device Identifiers

Device Issuing Agency	Device ID
GS1	05056619800390 [Primary]

FDA Product Code

• OVD: Intervertebral Fusion Device With Integrated Fixation, Lumbar

Sterilization

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

[05056619800390]

Moist Heat or Steam Sterilization

[05056619800390]

Moist Heat or Steam Sterilization

[05056619800390]

Moist Heat or Steam Sterilization

[05056619800390]

Moist Heat or Steam Sterilization

[05056619800390]

Moist Heat or Steam Sterilization

[05056619800390]

Moist Heat or Steam Sterilization

[05056619800390]

Moist Heat or Steam Sterilization

[05056619800390]

Moist Heat or Steam Sterilization

[05056619800390]

Moist Heat or Steam Sterilization

[05056619800390]

Moist Heat or Steam Sterilization

[05056619800390]

Moist Heat or Steam Sterilization

[05056619800390]

Moist Heat or Steam Sterilization

[05056619800390]

Moist Heat or Steam Sterilization

[05056619800390]

Moist Heat or Steam Sterilization

[05056619800390]

Moist Heat or Steam Sterilization

[05056619800390]

Moist Heat or Steam Sterilization

Device Entry Metadata

• Public Version Status: New
• Device Record Status: Published
• Public Version Number: 1
• Public Version Date: 2023-05-25
• Device Publish Date: 2023-05-17

On-Brand Devices [Axis Spine Technologies ALIF System Instrument]

• 05060771809900: ALIF Endplate Alignment Tool
• 05060771809894: Disc Spreader Tip (Medium Straight)
• 05060771809887: Disc Spreader Tip (Small Straight)
• 05060771809870: ALIF Slim Tamp
• 05060771809863: Disc Spreader
• 05060771809672: Disc Spreader Tip (Medium Angled Right)
• 05060771809665: Disc Spreader Tip (Medium Angled Left)
• 05060771809658: Disc Spreader Tip (Small Angled Right)
• 05060771809641: Disc Spreader Tip (Small Angled Left)
• 05060771809597: ALIF Graft Tamp
• 05060771809580: ALIF Loading Block
• 05060771809207: T Handle (Sq)
• 05060771808712: ALIF Endplate Sizer Large Slim
• 05060771808705: ALIF Endplate Sizer Small Slim
• 05060771808699: ALIF Endplate Sizer Medium Slim
• 05060771807760: ALIF Tamp
• 05060771806534: ALIF Blocker Plate Remover
• 05060771806510: ALIF Inserter (Superior)
• 05060771806473: ALIF Core Trial - 8x30
• 05060771806459: ALIF Core Trial - 6x30
• 05060771806350: ALIF Core Trial - 8x25
• 05060771806336: ALIF Core Trial - 6x25
• 05060771806251: ALIF Core Trial - 10x20
• 05060771806237: ALIF Core Trial - 8x20
• 05060771806213: ALIF Core Trial - 6x20
• 05060771806138: ALIF Core Trial - 10x15
• 05060771806114: ALIF Core Trial - 8x15
• 05060771806091: ALIF Core Trial - 6x15
• 05060771806015: ALIF Core Trial - 10x10
• 05060771805995: ALIF Core Trial - 8x10
• 05060771805971: ALIF Core Trial - 6x10
• 05060771804608: ALIF Endplate Sizer Large
• 05060771804592: ALIF Endplate Sizer Small
• 05060771804585: ALIF Endplate Sizer Medium
• 05060771804110: Straight Handle (Small AO)
• 05060771804103: ALIF Angled Screw Inserter Anti-Torque
• 05060771804042: ALIF Angled Screw Inserter
• 05060771804028: ALIF Screwdriver
• 05060771804011: T-Handle Small AO
• 05060771803748: ALIF Graft Syringe Medium
• 05060771803588: ALIF Slap Hammer
• 05060771803502: ALIF Graft Syringe Small
• 05056619801052: ALIF Core Loader
• 05056619801045: Paddle Distractor 12mm
• 05056619801038: Slotted Mallet
• 05056619801007: ALIF Curved Awl Long
• 05056619800994: ALIF Core Trial Inserter
• 05056619800826: ALIF Inserter Inferior
• 05056619800819: ALIF Inserter Superior
• 05056619800802: Disc Spreader Tip (Laminar Angled Right)