OptiCross 6

GUDID 08714729904762

Coronary Imaging Catheter

BOSTON SCIENTIFIC CORPORATION

Intravascular ultrasound imaging catheter, single-use

• Primary Device ID: 08714729904762
• NIH Device Record Key: 2a958cd8-2eb2-4f37-8da3-6a6a5a1b8b28
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: OptiCross 6
• Version Model Number: H7495181160
• 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: true
• 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	08714729904762 [Primary]

FDA Product Code

• OBJ: Catheter, ultrasound, intravascular

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: 2020-02-11
• Device Publish Date: 2016-09-24

On-Brand Devices [OptiCross 6]

• 08714729904762: Coronary Imaging Catheter
• 08714729904755: Coronary Imaging Catheter