BRITECROSS™ Support Catheter BC35135

GUDID 20705032101117

BriteCross .035 x 135CM

Cordis US Corp.

Vascular guide-catheter, single-use

• Primary Device ID: 20705032101117
• NIH Device Record Key: 604ba4e6-af39-45c2-a72c-8e21afb967c6
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: BRITECROSS™ Support Catheter
• Version Model Number: BC35135
• Catalog Number: BC35135
• Company DUNS: 118274128
• Company Name: Cordis US Corp.
• 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 Identifiers

Device Issuing Agency	Device ID
GS1	20705032101117 [Primary]

FDA Pre-market Approvals/Notifications & deNovo

• Premarket Notification: K233637

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: 2025-09-09
• Device Publish Date: 2025-09-01

On-Brand Devices [BRITECROSS™ Support Catheter]

• 20705032101124: BriteCross .035 x 190CM
• 20705032101117: BriteCross .035 x 135CM
• 20705032101100: BriteCross .035 x 90CM
• 20705032101094: BriteCross .018 x 200CM
• 20705032101087: BriteCross .018 x 150CM
• 20705032101070: BriteCross .018 x 90CM
• 20705032101063: BriteCross .018 x 65CM
• 20705032101056: BriteCross .014 x 200CM
• 20705032101049: BriteCross .014 x 150CM
• 20705032101032: BriteCross .014 x 90CM
• 20705032101025: BriteCross .014 x 65CM