CROSSWAY

GUDID 00889095740998

Channel Guide, Right 10°

GLOBUS MEDICAL, INC.

Orthopaedic surgical procedure kit, non-medicated, reusable

• Primary Device ID: 00889095740998
• NIH Device Record Key: b23e5c13-7ac2-449d-8f7d-324dd093e369
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: CROSSWAY
• Version Model Number: 6177.1610
• Company DUNS: 139105691
• Company Name: GLOBUS MEDICAL, INC.
• 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: false
• OTC Over-The-Counter: false

Customer Support Contacts

• Phone: +1(610)930-1800
• Email: info@globusmedical.com

Device Dimensions

• Angle: 10 degree

Device Identifiers

Device Issuing Agency	Device ID
GS1	00889095740998 [Primary]

FDA Product Code

• HRX: Arthroscope

Sterilization

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

[00889095740998]

Moist Heat or Steam Sterilization

Device Entry Metadata

• Public Version Status: New
• Device Record Status: Published
• Public Version Number: 1
• Public Version Date: 2019-07-22
• Device Publish Date: 2019-07-12

On-Brand Devices [CROSSWAY]

• 00889095998696: Adjustable Depth Stop, 18-26mm
• 00889095998689: Harvesting Mill, 6mm
• 00889095998634: Temporary Fixation Screw, 10mm
• 00889095741025: Adjustable Depth Stop, 10-18mm
• 00889095740998: Channel Guide, Right 10°
• 00889095740981: Adjustable Channel Guide
• 00889095740974: Channel Guide, Left 10°
• 00889095740929: Fixation Screw Driver
• 00889095998672: Pilot Drill, 2mm
• 00889095998658: Temporary Fixation Screw, 14mm
• 00889095998641: Temporary Fixation Screw, 12mm
• 00889095998665: Temporary Fixation Screw, 16mm