SCARLET AL-T SCA-LL 05 18-S

GUDID 07640221370396

Secured Lumbar Anterior Cage

SpineArt SA

Metallic spinal interbody fusion cage

• Primary Device ID: 07640221370396
• NIH Device Record Key: 11c155f3-5cf6-47f1-91cc-93276149721e
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: SCARLET AL-T
• Version Model Number: SCA-LL 05 18-S
• Catalog Number: SCA-LL 05 18-S
• Company DUNS: 483016148
• Company Name: SpineArt SA
• Device Count: 1
• DM Exempt: false
• Pre-market Exempt: false
• MRI Safety Status: MR Conditional
• Human Cell/Tissue Product: false
• Device Kit: false
• Device Combination Product: false
• Single Use: true
• Lot Batch: true
• Serial Number: false
• Manufacturing Date: true
• Expiration Date: true
• Donation Id Number: false
• Contains Natural Rubber Latex: false
• Labeled No Natural Rubber Latex: false
• RX Perscription: true
• OTC Over-The-Counter: false

Device Dimensions

• Angle: 5 degree
• Height: 18 Millimeter
• Angle: 5 degree
• Height: 18 Millimeter
• Angle: 5 degree
• Height: 18 Millimeter
• Angle: 5 degree
• Height: 18 Millimeter
• Angle: 5 degree
• Height: 18 Millimeter
• Angle: 5 degree
• Height: 18 Millimeter
• Angle: 5 degree
• Height: 18 Millimeter
• Angle: 5 degree
• Height: 18 Millimeter
• Angle: 5 degree
• Height: 18 Millimeter
• Angle: 5 degree
• Height: 18 Millimeter
• Angle: 5 degree
• Height: 18 Millimeter
• Angle: 5 degree
• Height: 18 Millimeter

Device Identifiers

Device Issuing Agency	Device ID
GS1	07640221370396 [Primary]

FDA Product Code

• MAX: Intervertebral Fusion Device With Bone Graft, Lumbar

Sterilization

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

Device Entry Metadata

• Public Version Status: New
• Device Record Status: Published
• Public Version Number: 1
• Public Version Date: 2025-06-19
• Device Publish Date: 2025-06-11

On-Brand Devices [SCARLET AL-T]

• 07640375235718: UNIVERSAL IMPLANT INSERTER
• 07640332479995: TRIAL MEDIUM
• 07640332479988: TRIAL MEDIUM
• 07640332479971: TRIAL MEDIUM
• 07640332479964: TRIAL MEDIUM
• 07640332479957: TRIAL MEDIUM
• 07640332479940: TRIAL SMALL
• 07640332479933: TRIAL SMALL
• 07640332479926: TRIAL SMALL
• 07640332479919: TRIAL SMALL
• 07640332479902: TRIAL SMALL
• 07640332479896: TRIAL SMALL
• 07640332479889: TRIAL SMALL
• 07640332479872: TRIAL SMALL
• 07640332479865: TRIAL LARGE
• 07640332479858: TRIAL LARGE
• 07640332479841: TRIAL MEDIUM
• 07640332479834: TRIAL MEDIUM
• 07640332479827: TRIAL SMALL
• 07640332479810: TRIAL SMALL
• 07640221370402: Secured Lumbar Anterior Cage
• 07640221370396: Secured Lumbar Anterior Cage
• 07640221370389: Secured Lumbar Anterior Cage
• 07640221370372: Secured Lumbar Anterior Cage
• 07640221370365: Secured Lumbar Anterior Cage
• 07640221370358: Secured Lumbar Anterior Cage
• 07640221370341: Secured Lumbar Anterior Cage
• 07640221370334: Secured Lumbar Anterior Cage
• 07640221370327: Secured Lumbar Anterior Cage
• 07640221370310: Secured Lumbar Anterior Cage
• 07640221370303: Secured Lumbar Anterior Cage
• 07640221370297: Secured Lumbar Anterior Cage
• 07640221370280: Secured Lumbar Anterior Cage
• 07640221370273: Secured Lumbar Anterior Cage
• 07640221370266: Secured Lumbar Anterior Cage
• 07640221370259: Secured Lumbar Anterior Cage
• 07640221370242: Secured Lumbar Anterior Cage
• 07640221370235: Secured Lumbar Anterior Cage
• 07640221370228: Secured Lumbar Anterior Cage
• 07640221370211: Secured Lumbar Anterior Cage
• 07640221370204: Secured Lumbar Anterior Cage
• 07640221370198: Secured Lumbar Anterior Cage
• 07640221370181: Secured Lumbar Anterior Cage
• 07640221370174: Secured Lumbar Anterior Cage
• 07640221370167: Secured Lumbar Anterior Cage
• 07640221370150: Secured Lumbar Anterior Cage
• 07640221370143: Secured Lumbar Anterior Cage
• 07640221370136: Secured Lumbar Anterior Cage
• 07640221370129: Secured Lumbar Anterior Cage
• 07640221370112: Secured Lumbar Anterior Cage