Cable, IntellaTip MiFi™ OI M0046270

GUDID 08714729877424

Sterile Cable

BOSTON SCIENTIFIC CORPORATION

Electrical-only medical device connection cable, reusable

• Primary Device ID: 08714729877424
• NIH Device Record Key: 4a198fc5-b0f6-4dba-82a7-1eeb46a8d128
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: Cable, IntellaTip MiFi™ OI
• Version Model Number: M0046270
• Catalog Number: M0046270
• 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 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 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 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	08714729877424 [Primary]

FDA Pre-market Approvals/Notifications & deNovo

• Premarket Approval: P150005

FDA Product Code

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

Sterilization

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

[08714729877424]

Ethylene Oxide;Moist Heat or Steam Sterilization

[08714729877424]

Ethylene Oxide;Moist Heat or Steam Sterilization

[08714729877424]

Ethylene Oxide;Moist Heat or Steam Sterilization

[08714729877424]

Ethylene Oxide;Moist Heat or Steam Sterilization

[08714729877424]

Ethylene Oxide;Moist Heat or Steam Sterilization

[08714729877424]

Ethylene Oxide;Moist Heat or Steam Sterilization

[08714729877424]

Ethylene Oxide;Moist Heat or Steam Sterilization

[08714729877424]

Ethylene Oxide;Moist Heat or Steam Sterilization

[08714729877424]

Ethylene Oxide;Moist Heat or Steam Sterilization

[08714729877424]

Ethylene Oxide;Moist Heat or Steam Sterilization

[08714729877424]

Ethylene Oxide;Moist Heat or Steam Sterilization

[08714729877424]

Ethylene Oxide;Moist Heat or Steam Sterilization

Device Entry Metadata

• Public Version Status: Update
• Device Record Status: Published
• Public Version Number: 4
• Public Version Date: 2025-06-30
• Device Publish Date: 2017-03-15

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• 08714729339830 - Percuflex™: 2026-02-17 Ureteral Stent Set
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• 08714729424222 - Contour™: 2026-02-17 Ureteral Stent Set