Advisor™ VL D-AVSE-D20-V1525

GUDID 05415067027269

Circular Mapping Catheter

ST. JUDE MEDICAL, INC.

Cardiac mapping catheter, percutaneous, single-use

• Primary Device ID: 05415067027269
• NIH Device Record Key: 4cc9483c-90f5-45eb-b8de-68d8902d8db9
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: Advisor™ VL
• Version Model Number: Sensor Enabled™
• Catalog Number: D-AVSE-D20-V1525
• Company DUNS: 149818952
• Company Name: ST. JUDE MEDICAL, INC.
• 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

• Length: 117 Centimeter

Operating and Storage Conditions

• Storage Environment Temperature: Between -20 Degrees Celsius and 50 Degrees Celsius

Device Identifiers

Device Issuing Agency	Device ID
GS1	05415067027269 [Primary]

FDA Pre-market Approvals/Notifications & deNovo

• Premarket Notification: K192037

FDA Product Code

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

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: 2019-10-04
• Device Publish Date: 2019-09-26

On-Brand Devices [Advisor™ VL]

• 05415067027283: Circular Mapping Catheter
• 05415067027276: Circular Mapping Catheter
• 05415067027269: Circular Mapping Catheter
• 05415067027252: Circular Mapping Catheter