FilterWire EZ™

GUDID 08714729470861

Embolic Protection System

BOSTON SCIENTIFIC CORPORATION

Embolic protection filtering guidewire

• Primary Device ID: 08714729470861
• NIH Device Record Key: b4fc865d-1f8d-4df8-83b0-ae48929525a8
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: FilterWire EZ™
• Version Model Number: H749201003000
• Company DUNS: 021717889
• Company Name: BOSTON SCIENTIFIC 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

Device Dimensions

• Device Size Text, specify: 0

Device Identifiers

Device Issuing Agency	Device ID
GS1	08714729470861 [Primary]

FDA Product Code

• NFA: Temporary Coronary Saphenous Vein Bypass Graft for Embolic Protection

Sterilization

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

Device Entry Metadata

• Public Version Status: Update
• Device Record Status: Published
• Public Version Number: 3
• Public Version Date: 2019-04-09
• Device Publish Date: 2016-09-24

On-Brand Devices [FilterWire EZ™]

• 08714729808817: Embolic Protection System
• 08714729808800: Embolic Protection System
• 08714729470861: Embolic Protection System
• 08714729470854: Embolic Protection System