AXS Lift LIFT074105-01

GUDID 07613327623352

Intracranial Base Catheter

Stryker Corporation

Vascular guide-catheter, single-use

• Primary Device ID: 07613327623352
• NIH Device Record Key: fbb3f9d2-0ddd-492d-a623-24b4311523bd
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: AXS Lift
• Version Model Number: LIFT074105-01
• Catalog Number: LIFT074105-01
• Company DUNS: 042405446
• Company Name: Stryker Corporation
• 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: true
• 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(855)916-3876
• Email: NVCustomerService@stryker.com
• Phone: +1(855)916-3876
• Email: NVCustomerService@stryker.com
• Phone: +1(855)916-3876
• Email: NVCustomerService@stryker.com

Device Dimensions

• Lumen/Inner Diameter: 0.074 Inch
• Length: 105 Centimeter
• Lumen/Inner Diameter: 0.074 Inch
• Length: 105 Centimeter
• Lumen/Inner Diameter: 0.074 Inch
• Length: 105 Centimeter

Operating and Storage Conditions

• Special Storage Condition, Specify: Between 0 and 0 *Store in a cool, dry, dark place.
• Special Storage Condition, Specify: Between 0 and 0 *Store in a cool, dry, dark place.
• Special Storage Condition, Specify: Between 0 and 0 *Store in a cool, dry, dark place.

Device Identifiers

Device Issuing Agency	Device ID
GS1	07613327623352 [Primary]

FDA Pre-market Approvals/Notifications & deNovo

• Premarket Notification: K243593

FDA Product Code

• DQY: Catheter, percutaneous

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: 2025-03-12
• Device Publish Date: 2025-03-04

On-Brand Devices [AXS Lift]

• 07613327623390: Intracranial Base Catheter
• 07613327623376: Intracranial Base Catheter
• 07613327623352: Intracranial Base Catheter
• 07613327623338: Intracranial Base Catheter