CROSSER® GEN200

GUDID 00801741067617

CROSSER® Generator

Bard Peripheral Vascular, Inc.

Mechanical atherectomy system generator, electrical output

• Primary Device ID: 00801741067617
• NIH Device Record Key: c0969c0f-36cd-47dc-bea3-6ef156e8f0bf
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: CROSSER®
• Version Model Number: GEN200
• Catalog Number: GEN200
• Company DUNS: 135057938
• Company Name: Bard Peripheral Vascular, 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: false
• Serial Number: true
• Manufacturing Date: true
• 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(800)321-4254
• Email: medical.services@crbard.com
• Phone: +1(800)321-4254
• Email: medical.services@crbard.com

Device Identifiers

Device Issuing Agency	Device ID
GS1	00801741067617 [Primary]

FDA Product Code

• PDU: Catheter for crossing total occlusions

Sterilization

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

Device Entry Metadata

• Public Version Status: Update
• Device Record Status: Published
• Public Version Number: 3
• Public Version Date: 2018-09-24
• Device Publish Date: 2016-09-13

On-Brand Devices [CROSSER®]

• 00801741067617: CROSSER® Generator
• 00801741067471: CROSSER® System Foot Switch