CrossFlow 0450000500

GUDID 07613327058062

Footswitch

STRYKER CORPORATION

Foot-switch, electrical

• Primary Device ID: 07613327058062
• NIH Device Record Key: 3f6cc3d1-cc2b-4ce5-8dd7-d7ffcb14ff0e
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: CrossFlow
• Version Model Number: 0450000500
• Catalog Number: 0450000500
• Company DUNS: 187502109
• 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: false
• Lot Batch: false
• Serial Number: true
• 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: +1(866)624-4422
• Email: xx@xx.xx

Device Identifiers

Device Issuing Agency	Device ID
GS1	07613327058062 [Primary]

FDA Product Code

• HRX: ARTHROSCOPE

Sterilization

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

Device Entry Metadata

• Public Version Status: Update
• Device Record Status: Published
• Public Version Number: 2
• Public Version Date: 2018-03-29
• Device Publish Date: 2016-09-23

On-Brand Devices [CrossFlow]

• 37613327261036: Patient-Use Tubing, Do not use if package is damaged
• 37613327261029: Day-Use Inflow Cassette Tubing, Do not use if package is damaged
• 07613327058079: Stryker Console Customizer
• 07613327058062: Footswitch
• 07613327058048: Integrated Arthroscopy Pump
• 37613327055222: Integrated Cassette Tubing, Do not use if package is damaged
• 37613327055215: Outflow Cassette Tubing, Do not use if package is damaged
• 37613327055208: Inflow Cassette Tubing, Do not use if package is damaged