IntellaTip MiFi™ XP M004PM47900

GUDID 08714729848042

Temperature Ablation Catheter

BOSTON SCIENTIFIC CORPORATION

Cardiac radio-frequency ablation system catheter

• Primary Device ID: 08714729848042
• NIH Device Record Key: f7c66eac-cce8-472d-a866-9415152a1262
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: IntellaTip MiFi™ XP
• Version Model Number: M004PM47900
• Catalog Number: M004PM47900
• 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

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Device Identifiers

Device Issuing Agency	Device ID
GS1	08714729848042 [Primary]

FDA Pre-market Approvals/Notifications & deNovo

• Premarket Approval: P020025

FDA Product Code

• OAD: catheter, percutaneous, cardiac ablation, for treatment of atrial flutter

Sterilization

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

Device Entry Metadata

• Public Version Status: Update
• Device Record Status: Published
• Public Version Number: 5
• Public Version Date: 2021-09-16
• Device Publish Date: 2014-09-24

On-Brand Devices [IntellaTip MiFi™ XP]

• 08714729863243: Temperature Ablation Catheter
• 08714729848059: Temperature Ablation Catheter
• 08714729848042: Temperature Ablation Catheter
• 08714729848035: Temperature Ablation Catheter
• 08714729848028: Temperature Ablation Catheter
• 08714729848011: Temperature Ablation Catheter