Reflexion Spiral™ D402865

GUDID 05414734206211

ST. JUDE MEDICAL CARDIOVASCULAR DIVISION

Cardiac mapping catheter, percutaneous, single-use

• Primary Device ID: 05414734206211
• NIH Device Record Key: ccbe09e3-1fbd-4002-b412-ea29c2c0b485
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: Reflexion Spiral™
• Version Model Number: Bi-Directional Variable Radius Catheter
• Catalog Number: D402865
• Company DUNS: 040960379
• Company Name: ST. JUDE MEDICAL CARDIOVASCULAR DIVISION
• 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: true
• 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

Customer Support Contacts

• Phone: +1(855)478-5833
• Email: customerservice@sjm.com

Device Dimensions

• Catheter Gauge: 7 French

Operating and Storage Conditions

• Special Storage Condition, Specify: Between 0 and 0 *Store in a cool dark, dry, place. Do not use if package is damaged.

Device Identifiers

Device Issuing Agency	Device ID
GS1	05414734206211 [Primary]

FDA Pre-market Approvals/Notifications & deNovo

• Premarket Notification: K072012

FDA Product Code

• DRF: CATHETER, ELECTRODE RECORDING, OR PROBE, ELECTRODE RECORDING

Sterilization

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

Device Entry Metadata

• Public Version Status: Update
• Device Record Status: Published
• Public Version Number: 3
• Public Version Date: 2018-07-06
• Device Publish Date: 2016-01-28

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