IntellaTip MiFi™ Filter Module

GUDID 08714729847939

RF Frequency Filter

BOSTON SCIENTIFIC CORPORATION

Electronic signal frequency filter Electronic signal frequency filter Electronic signal frequency filter Electronic signal frequency filter Electronic signal frequency filter Electronic signal frequency filter Electronic signal frequency filter Electronic signal frequency filter Electronic signal frequency filter Electronic signal frequency filter Electronic signal frequency filter Electronic signal frequency filter Electronic signal frequency filter Electronic signal frequency filter

• Primary Device ID: 08714729847939
• NIH Device Record Key: bf43a39d-3a34-46ec-ade8-1792f286972a
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: IntellaTip MiFi™ Filter Module
• Version Model Number: M00412120
• 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: true
• Device Combination Product: false
• Single Use: false
• Lot Batch: false
• Serial Number: true
• Manufacturing Date: true
• Expiration Date: false
• 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	08714729847939 [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: false

Device Entry Metadata

• Public Version Status: Update
• Device Record Status: Published
• Public Version Number: 4
• Public Version Date: 2023-10-19
• Device Publish Date: 2014-09-24

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