EASYTRAK® 3

GUDID 00802526353871

Coronary Venous Steroid-Eluting Bipolar Pace/Sense Lead

BOSTON SCIENTIFIC CORPORATION

Endocardial pacing lead

• Primary Device ID: 00802526353871
• NIH Device Record Key: fc6fd71f-2d96-4364-9901-35d7af1a5b45
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: EASYTRAK® 3
• Version Model Number: 4527
• Company DUNS: 106295384
• Company Name: BOSTON SCIENTIFIC CORPORATION
• Device Count: 1
• 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: true
• Single Use: true
• Lot Batch: false
• Serial Number: true
• 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

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Device Identifiers

Device Issuing Agency	Device ID
GS1	00802526353871 [Primary]

FDA Pre-market Approvals/Notifications & deNovo

• Premarket Approval: P010012

FDA Product Code

• NIK: Defibrillator, automatic implantable cardioverter, with cardiac resynchronization (CRT-D)

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: 2018-07-06
• Device Publish Date: 2014-09-24

On-Brand Devices [EASYTRAK® 3]

• 00802526353871: Coronary Venous Steroid-Eluting Bipolar Pace/Sense Lead
• 00802526353772: Coronary Venous Steroid-Eluting Bipolar Pace/Sense Lead
• 00802526353758: Coronary Venous Steroid-Eluting Bipolar Pace/Sense Lead