Cable, IntellaNav™ Ablation Catheter M004RARC010

GUDID 08714729848783

Sterile Cable

BOSTON SCIENTIFIC CORPORATION

Electrical-only medical device connection cable, reusable

• Primary Device ID: 08714729848783
• NIH Device Record Key: 61c9b24f-0ebf-4ccf-acb2-03b4a7c78f52
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: Cable, IntellaNav™ Ablation Catheter
• Version Model Number: M004RARC010
• Catalog Number: M004RARC010
• 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: false
• 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 Dimensions

• Device Size Text, specify: 0
• Device Size Text, specify: 0
• Device Size Text, specify: 0
• Device Size Text, specify: 0
• Device Size Text, specify: 0
• Device Size Text, specify: 0

Device Identifiers

Device Issuing Agency	Device ID
GS1	08714729848783 [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: true
• Device Is Sterile: true

[08714729848783]

Hydrogen Peroxide;Ethylene Oxide;Moist Heat or Steam Sterilization

[08714729848783]

Hydrogen Peroxide;Ethylene Oxide;Moist Heat or Steam Sterilization

[08714729848783]

Hydrogen Peroxide;Ethylene Oxide;Moist Heat or Steam Sterilization

Device Entry Metadata

• Public Version Status: Update
• Device Record Status: Published
• Public Version Number: 5
• Public Version Date: 2026-02-24
• Device Publish Date: 2016-03-18

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