Axis Spine Technologies ALIF Implant 1984-00-105

GUDID 05060771807906

Superior Endplate Hyper Lordotic (5) - Medium

AXIS SPINE TECHNOLOGIES LTD

Metallic spinal interbody fusion cage

• Primary Device ID: 05060771807906
• NIH Device Record Key: 5b91c862-a05d-4fbb-a63e-9d542e455ecc
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: Axis Spine Technologies ALIF Implant
• Version Model Number: 1984-00-105
• Catalog Number: 1984-00-105
• 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: 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: +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	05060771807906 [Primary]

FDA Product Code

• OVD: Intervertebral Fusion Device With Integrated Fixation, Lumbar

Sterilization

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

[05060771807906]

Moist Heat or Steam Sterilization

[05060771807906]

Moist Heat or Steam Sterilization

[05060771807906]

Moist Heat or Steam Sterilization

[05060771807906]

Moist Heat or Steam Sterilization

[05060771807906]

Moist Heat or Steam Sterilization

[05060771807906]

Moist Heat or Steam Sterilization

[05060771807906]

Moist Heat or Steam Sterilization

[05060771807906]

Moist Heat or Steam Sterilization

[05060771807906]

Moist Heat or Steam Sterilization

[05060771807906]

Moist Heat or Steam Sterilization

[05060771807906]

Moist Heat or Steam Sterilization

[05060771807906]

Moist Heat or Steam Sterilization

[05060771807906]

Moist Heat or Steam Sterilization

[05060771807906]

Moist Heat or Steam Sterilization

[05060771807906]

Moist Heat or Steam Sterilization

[05060771807906]

Moist Heat or Steam Sterilization

Device Entry Metadata

• Public Version Status: New
• Device Record Status: Published
• Public Version Number: 1
• Public Version Date: 2023-05-24
• Device Publish Date: 2023-05-16

On-Brand Devices [Axis Spine Technologies ALIF Implant]

• 05060771807920: Superior Endplate Hyper Lordotic (5) - Large
• 05060771807906: Superior Endplate Hyper Lordotic (5) - Medium
• 05060771807876: Inferior Endplate Hyper Lordotic (5) - Large
• 05060771807821: Inferior Endplate Coronal Right (5) - Large
• 05060771807814: Inferior Endplate Coronal Left (5) - Large
• 05060771807807: Superior Endplate Coronal Right (5) - Large
• 05060771807791: Superior Endplate Coronal Left (5) - Large
• 05060771807784: Inferior Endplate - Large
• 05060771807777: Superior Endplate - Large
• 05060771807623: Locking Cap M/L 10 x 20
• 05060771807609: Locking Cap M/L 10 x 15
• 05060771807586: Locking Cap M/L 10 x 10
• 05060771807487: Locking Cap M/L 8 x 30
• 05060771807463: Locking Cap M/L 8 x 25
• 05060771807449: Locking Cap M/L 8 x 20
• 05060771807425: Locking Cap M/L 8 x 15
• 05060771807401: Locking Cap M/L 8 x 10
• 05060771807302: Locking Cap M/L 6 x 30
• 05060771807289: Locking Cap M/L 6 x 25
• 05060771807265: Locking Cap M/L 6 x 20
• 05060771807241: Locking Cap M/L 6 x 15
• 05060771807227: Locking Cap M/L 6 x10
• 05060771807210: Screw H20 - 35mm
• 05060771807203: Screw H20 - 32.5mm
• 05060771807197: Screw H20 - 30mm
• 05060771807180: Screw H20 - 27.5mm
• 05060771807173: Screw H20 - 25mm
• 05060771807159: Screw H20 - 20mm
• 05060771807111: Core M/L 10 x 20
• 05060771807104: Core M/L 10 x 15
• 05060771807098: Core M/L 10 x 10
• 05060771807081: Core M/L 8 x 30
• 05060771807074: Core M/L 8 x 25
• 05060771807067: Core M/L 8 x 20
• 05060771807050: Core M/L 8 x 15
• 05060771807043: Core M/L 8 x 10
• 05060771807036: Core M/L 6 x 30
• 05060771807029: Core M/L 6 x 25
• 05060771807012: Core M/L 6 x 20
• 05060771807005: Core M/L 6 x 15
• 05060771806992: Core M/L 6 x10
• 05060771806961: Inferior Endplate Hyper Lordotic (5) - Medium
• 05060771806916: Inferior Endplate Coronal Right (5) - Medium
• 05060771806909: Inferior Endplate Coronal Left (5) - Medium
• 05060771806893: Superior Endplate Coronal Right (5) - Medium
• 05060771806886: Superior Endplate Coronal Left (5) - Medium
• 05060771806879: Inferior Endplate - Medium
• 05060771806862: Superior Endplate - Medium
• 05060771807937: Superior Endplate Hyper Lordotic (10) - Large
• 05060771807913: Superior Endplate Hyper Lordotic (10) - Medium