Rubicon™ Control H749394321413A0

GUDID 00191506019594

Support Catheter

BOSTON SCIENTIFIC CORPORATION

Vascular guide-catheter, single-use Vascular guide-catheter, single-use Vascular guide-catheter, single-use Vascular guide-catheter, single-use Vascular guide-catheter, single-use Vascular guide-catheter, single-use Vascular guide-catheter, single-use Vascular guide-catheter, single-use Vascular guide-catheter, single-use Vascular guide-catheter, single-use Vascular guide-catheter, single-use Vascular guide-catheter, single-use Vascular guide-catheter, single-use Vascular guide-catheter, single-use Vascular guide-catheter, single-use Vascular guide-catheter, single-use Vascular guide-catheter, single-use

• Primary Device ID: 00191506019594
• NIH Device Record Key: 1340731e-7055-4f6e-938d-1150bb3af94a
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: Rubicon™ Control
• Version Model Number: H749394321413A0
• Catalog Number: H749394321413A0
• 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

• Catheter Length: 135 Centimeter
• Guidewire Diameter: 0.014 Inch
• Catheter Length: 135 Centimeter
• Guidewire Diameter: 0.014 Inch
• Catheter Length: 135 Centimeter
• Guidewire Diameter: 0.014 Inch
• Catheter Length: 135 Centimeter
• Guidewire Diameter: 0.014 Inch
• Catheter Length: 135 Centimeter
• Guidewire Diameter: 0.014 Inch
• Catheter Length: 135 Centimeter
• Guidewire Diameter: 0.014 Inch
• Catheter Length: 135 Centimeter
• Guidewire Diameter: 0.014 Inch
• Catheter Length: 135 Centimeter
• Guidewire Diameter: 0.014 Inch
• Catheter Length: 135 Centimeter
• Guidewire Diameter: 0.014 Inch
• Catheter Length: 135 Centimeter
• Guidewire Diameter: 0.014 Inch
• Catheter Length: 135 Centimeter
• Guidewire Diameter: 0.014 Inch
• Catheter Length: 135 Centimeter
• Guidewire Diameter: 0.014 Inch
• Catheter Length: 135 Centimeter
• Guidewire Diameter: 0.014 Inch
• Catheter Length: 135 Centimeter
• Guidewire Diameter: 0.014 Inch
• Catheter Length: 135 Centimeter
• Guidewire Diameter: 0.014 Inch
• Catheter Length: 135 Centimeter
• Guidewire Diameter: 0.014 Inch
• Catheter Length: 135 Centimeter
• Guidewire Diameter: 0.014 Inch

Device Identifiers

Device Issuing Agency	Device ID
GS1	00191506019587 [Primary]
GS1	00191506019594 [Package]; Contains: 00191506019587; Package: [5 Units]; In Commercial Distribution

FDA Product Code

• DQY: Catheter, percutaneous

Sterilization

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

Device Entry Metadata

• Public Version Status: New
• Device Record Status: Published
• Public Version Number: 1
• Public Version Date: 2024-02-26
• Device Publish Date: 2024-02-16

On-Brand Devices [Rubicon™ Control]

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• 00191506019877: Support Catheter
• 00191506019853: Support Catheter
• 00191506019839: Support Catheter
• 00191506019815: Support Catheter
• 00191506019792: Support Catheter
• 00191506019778: Support Catheter
• 00191506019754: Support Catheter
• 00191506019730: Support Catheter
• 00191506019716: Support Catheter
• 00191506019693: Support Catheter
• 00191506019679: Support Catheter
• 00191506019655: Support Catheter
• 00191506019631: Support Catheter
• 00191506019617: Support Catheter
• 00191506019594: Support Catheter
• 00191506019570: Support Catheter