OptiCross™ HD H74939352040

GUDID 08714729960737

Coronary Imaging Catheter

BOSTON SCIENTIFIC CORPORATION

Intravascular ultrasound imaging catheter, single-use

• Primary Device ID: 08714729960737
• NIH Device Record Key: c960d057-f069-4914-8fae-30699d53d024
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: OptiCross™ HD
• Version Model Number: H74939352040
• Catalog Number: H74939352040
• 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: false
• 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	08714729960737 [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: 2018-02-06

On-Brand Devices [OptiCross™ HD]

• 08714729960768: Coronary Imaging Catheter
• 08714729960737: Coronary Imaging Catheter
• 00191506035419: Coronary Imaging Catheters